Can The Class Action Lawsuit Against Lance Armstrong Actually Work?

The Lance Armstrong saga continues (we've written on Lance HERE, HERE, HERE)... this week saw a class action lawsuit filed against Lance Armstrong and various publishers on behalf of California consumers who claim they were misled by Defendants' statements and purchased Defendant Armstrong's books based upon the false belief that they were true and honest works of nonfiction.

When I first heard about the class action, I immediately thought "Are you kidding me?  Sure, we'd all like to sue Oliver Stone for subjecting us to JFK in 10th grade history class but this? ... come on."

SO, is this class action against Lance Armstrong legit? Actually, it might be.

Stutzman, et al v Lance Armstrong, et al, filed January 22, 2013 in the US District Court for the Eastern District of California, alleges Lance Armstrong et al, made multiple misrepresentations contained in Lance Armstrong's books, IT'S NOT ABOUT THE BIKE: My JOURNEY BACK TO LIFE and EVERY SECOND COUNTS, and advertisements and marketing for the books (including the front and back cover and flyleafs media press kits, during television and newspaper interviews, on Internet websites and at personal appearances made by Armstrong) as true and honest works of nonfiction when, in fact, Defendants knew or should have known that these books were works of fiction. Further, the lawsuit claims Lance Armstrong et al advertised marketed and sold these books as a works of nonfiction.

The Plaintiffs allege they were misled by Lance Armstrong's and the other Defendants' statements and purchased Lance Armstrong's books based upon the false belief that they were true and honest works of nonfiction. In their 59-page Complaint, Plaintiffs cite to the exhaustive and growing body of evidence and recent admissions by Lance Armstrong himself to support the allegations of misrepresentation and fraud regarding Lance Armstrong’s use of banned substances (EPO, blood doping, testosterone) during his professional cycling career.

Knowing that the mere claim that his success was due to superior physical training, proper diet and an extraordinary spirit and drive to succeed was not enough to quell suspicions and rumors that he doped, Defendant Armstrong wrote lengthy passages in IT'S NOT ABOUT THE BIKE: My JOURNEY BACK TO LIFE that were intended to convince readers and consumers - including Plaintiffs and the members of the Class - that the rumors of Armstrong's doping were unfair and untrue because of the extensive drug-testing regime employed by the DCI and the organizers of the Tour de France... Complaint ¶ 20

In order to survive a motion to dismiss, the Plaintiffs will have to overcome the pleading requirements of Federal Rule of Civil Procedure 9(b) which requires state-law claims grounded in fraud to be plead with particularity and requires a plaintiff to plead with particularity the circumstances constituting the fraud while malice, intent, knowledge, and other conditions of a person's mind may be alleged generally. “Averments of fraud must be accompanied by the ‘who, what, when, where, and how’ of the misconduct charged.” Yess v. Ciba–Geigy Corp. USA; Villegas v. Wells Fargo Bank, N.A. (N.D. Cal. Sept. 17, 2012).

The Complaint almost certainly meets Rule 9(b)’s requirements as to Lance Armstrong. As to the other named Defendants however, the Plaintiffs may not get so far. This lawsuit was brought in a Federal Court in the Eastern District of California – a court within the jurisdiction of the 9th Circuit. The United States Court of Appeals for the 9th Circuit has held that a book publisher owed no duty to a car dealership owner for allegedly publishing errors concerning emission systems in automobiles. Sinai v. Mitchell Books (9th Cir.1993). In 2000, a New York court followed the 9th Circuit’s lead and supported the proposition that publishers have no duty to investigate the accuracy of its books.

The Sinai court stated that absent an express warranty, publishers have no duty to investigate the accuracy of the contents of the books it publishes and concluded that such a duty could not be created because a publisher's right to publish free of fear of liability is guaranteed by the First Amendment and the overriding societal interest in the untrammeled dissemination of knowledge. While the Sinai case is 20 years old and may be revisited or distinguished at this point, it may be that the “deep pockets” of the publishers in the case might not be reachable by the Plaintiffs. Which would leave Lance Armstrong alone to pay any judgment.

This case will be interesting to watch in light of Lance Armstrong's recent admissions, alleged recent lies, and anticipated flood of lawsuits resulting therefrom.  If the case is permitted to move forward it will no doubt be because of Lance Armstrong's years of agressive lies and denials about his drug use during his cycling career.  The crux of the case is the contention that the Plaintiffs would not have purchased the books had the truth not been withheld by Lance Armstrong. 

The Boulder Business Lawyers at Laszlo & Associates, LLC provide legal counsel for businesses on a variety of business needs, including products liability, risk management, corporate protection, and legal compliance.

What is A Sur-Reply? And When is Filing One Permitted?

Our blogs have been following the Lance Armstrong v. USADA, et al. case which is currently proceeding in the United States District Court for the Western District of Texas.  While the case presents intricate issues of constitutional due process; private versus state action; and enforceability of arbitration clauses, we have been intrigued by the technical and procedural issues the case has presented.  We wrote about pleading deadlines when Armstrong's attorneys miscalculated the response date ... and we discussed brief page limits when Armstrong asked for more space to argue his case.  Yesterday, Armstrong filed  a Sur-Reply in Opposition to USADA's Motion to Dismiss. 

First, what is a "Sur-Reply?"  A sur-reply is a reply filed in response to the reply to a motion… motions go like this: Motion >Response> Reply.  Party A ("movant") files a Motion that asks the court to do something and argues its position – Party B ("non-movant") files a response which argues against the Motion – Party A then files a Reply which supports the Motion – but Party A is limited to those arguments and law raised in its original Motion.  After the reply is filed, the issue is “fully briefed.” 

However, when the reply brief raises new material that was not included in the original motion, courts may permit the non-movant to respond to the new material in a “sur-reply.”  No authorization exists in the Federal Rules of Civil Procedure (or the local rules of Western District of Texas) that permit a sur-reply and therefore, the party wishing to file a sur-reply must motion the court for leave to file a sur-reply.  USDC WD Texas Local Rule 7(e)-(f) deals with responses and replies. 7(f) states: “A party may file a reply in support of a motion. Absent leave of court, no further submissions on the motion are allowed.”  Further, a motion for leave is it own motion, separate and distinct from the underlying motion, and therefore, under most local rules (and USDC WD Texas Local Rule CV-7 (i)) requires a “meet and confer" prior to filing.

So, what did Lance Armstrong file?  He filed a sur-reply brief – he did not comply with Local Rule 7 and file a motion asking the court for leave to file the sur-reply itself (strike one) and he did not comply with Local Rule 7(i) and meet and confer with USADA (strike two).  Further, Armstrong did not argue that a sur-reply brief was necessary under the circumstances of the case. He did not show that USADA had presented new material in its reply brief that it had not included in the original Motion to Dismiss. (strike three).  Thus, the Court should find that Armstrong’s surreply brief is improper and should be stricken.

Why did Armstrong’s legal team yet again disregard the local rules?  It’s anyone’s guess … but headed into today’s hearing, it’s my guess that Armstrong’s legal team is clearly trying (desperately so) to get as much information in front of the Court as possible.  Most likely, Judge Sparks read the sur-reply headed into today’s hearing – even if he says otherwise and doesn’t allow the filing to stand.  The goal by Armstrong being just to get it all out and argue like mad today.   

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.  For more information on our Boulder criminal defense practice, visit our website at www.laszlolaw.com/civil.  Contact one of our Boulder attorneys if you are need of assistance.

Did Lance Armstrong's Legal Team Miss a Critical Filing Deadline? Why Strict Compliance With Local Rules is Crucial.

UPDATE: Judge Sam Sparks gave Lance Armstrong until midnight tonight, August 3, to file his response. The Court DENIED Armstrong's request for an extension until August 6. Read Lance v. USADA, et al. Order Granting Extension Until Aug 3, 2012 HERE.  The Court was mindful that USADA's Motion to Dismiss is a dispositive motion, and stated that due to the finality of such a ruling on the Motion, Armstrong should be afforded the opportunity to fully brief the issue.

###

[Our sister blog The Boulder Criminal Law Advisor] has been following and writing (HERE and HERE) about the Lance Armstrong v. USADA, et al. case since it was filed.  Yesterday, in Lance Armstrong v. USADA, et al., Mr. Armstrong's legal team filed a Consent Motion Extension for Extension of Time and Request for Further Extension of Time wherein he requested until August 6, 2012 to respond to USADA's Motion to Dismiss.  Armstrong's lawyers believed they had until August 6, 2012 to respond - USADA contends they had until August 2, 2012 and today filed its Response to Motion for Extension asking the Court to deny the Motion for Extension.  USADA supported its Response with exhibits of last minute emails between Sean Breen, one of Lance Armstrong's lawyers, and USADA attorney Bill Bock that show Breen was mistaken on the calculation of time.

So, when was the response due?  Did Armstrong's legal team screw up?  Let's go through the analysis.

USADA filed its Motion to Dismiss on July 19, 2012.  A motion to dismiss is a dispositive motion.  Under USDC WD Texas Local Rule CV-7(e)(2) which states: “A response to a dispositive motion shall be filed not later than 14 days after the filing of the motion,” Armstrong had 14 days to respond to USADA’s Motion.  USDC WD Texas Local Rule CV-6 states “In computing any time period in any civil case, the provisions of Federal Rule of Civil Procedure 6, as amended, shall be applied.” Thus, Per Fed. Civ. Rule 6(a)(1)(A) you must “exclude the day of the event that triggers the period;” – in this case, the 19th of July.  Therefore, the 14 day time period started to run on the 20th of July.  Per Fed. Civ. Rule 6(a)(1)(B), you “count every day, including intermediate Saturdays, Sundays,  and legal holidays…” so, counting 14 days puts us at a due date of August 2, 2012.

NOW here is where things get interesting… we’re not done adding time.  Fed. Civ. Rule 6(d) is called “Additional Time After Certain Kinds of Service.”  And, the Rule states: “When a party may or must act within a specified time after service and service is made under Rule 5(b)(2)(C), (D), (E), or (F), 3 days are added after the period would otherwise expire under Rule 6(a).”  What does this mean?  Let’s go to Fed. Civ. Rule 5.  Generally, Rule 5(a) required USADA to serve the Motion to Dismiss on Lance Armstrong – which it did, under 5(b)(E) by “sending it by electronic means if the person consented in writing—in which event service is complete upon transmission…” when it filed it's Motion with the Court on July 19th. Confused yet? Don’t be.  Revisiting Rule 6(d) reminds us that because USADA made service under 5(b)(E), Lance Armstrong gets the addition time of three (3) days in which to respond.  Making his response due on Sunday, August 5, 2012 -- BUT, per Fed. Civ. Rule 6(a)(1)(C), which states: "... but if the last day is a Saturday, Sunday, or legal holiday, the period continues to run until the end of the next day that is not a Saturday, Sunday, or legal holiday," the response is due on Monday, August 6, 2012 -- essentially, papers aren't due on weekends or holidays.

So, Armstrong is good right?  WRONG.  Look again at USDC WD Texas Local Rule CV-7(e)(2) which states: “A response to a dispositive motion shall be filed not later than 14 days after the filing of the motion,” Armstrong had 14 days to respond to USADA’s Motion from the filing- not from the service. So Local CV-6 is inapplicable and therefore the above analysis is irrelevant.  Hate lawyers yet?  So, the entire analysis Armstrong's lawyers went through, while correct, did not apply in this case.

UPDATE:  Seem a bit ticky-tacky?  Well, this exact issue has been settled for quite sometime. Seventeen years ago, the Fifth Circuit Court of Appeals stated:
"[t]he correct inquiry is whether the required actions must be performed within a prescribed period of filing or of service.-If the action is to be taken after filing, the time for action begins to run from that date. If the act is to be taken from service, the three day extension of ... [Rule] 6(e) applies."  Pavone v. Mississippi Riverboat Amusement Corp., 52 F.3d 560, 566 (5th Cir. 1995).

Not only is this terribly embarrassing for Armstrong's legal team, there is no question this a huge set back for Armstrong - the Court could very easily refuse to permit him to file a Response at all.  UPDATE: Court granted extension until Midnight August 3, 2012.

Moreover, this is a great lesson on the sheer importance of familiarizing yourself with the peculiarities of the Local Rules in each court in which you practice.  Such a miscalculation could expose Armstrong's lawyers to a claim of legal malpractice.  Missing a deadline is serious business - and its avoidable.  However, even the sharpest lawyers may accidentally miss deadlines - in this case, laziness was not to blame.  I am quite confident there was great attention paid to the above analysis.  But, they missed it.  It would be good practice to always forget about the extra three days under Fed. Civ. Rule 6 when calculating your due dates - if you have 7 days, file in 7 ... 14? file in 14 ... better safe than sorry.

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.  For more information on our Boulder criminal defense practice, visit our website at www.laszlolaw.com/civil.  Contact one of our Boulder attorneys if you are need of assistance.

No Innovator Liability For Brand Name Drug Manufacturers

We have discussed in previous posts the Supreme Court’s decision in Pliva v. Mensing which had the effect of making generic drug manufacturer “immune” from state failure-to-warn claims.  In summary, Mensing held that because federal regulations prevented a generic drug manufacturer from effectuating a change to the labeling for a particular drug, the generic drug manufacturers could not be liable for failure-to-warn claims.  The rationale runs along these lines: If a generic drug manufacturer cannot change the warning label because of federal law, how can a generic manufacturer be liable under state law for the generic drug’s label failing to adequately warn the user when it was “powerless” to change that warning?

While a clear win for the generic drug manufacturers, Mensing caused some initial concerns for brand name drug manufacturers that worried the decision might be used to make them liable for injuries caused by generic drugs.  The logic here being that because the brand name drug manufacturer controls the warning label based federal law, the brand name manufacturer can effectuate a change to the labeling of a drug--which the generic drug manufacturer must then mirror according to federal regulations.  So a failure to warn of say a possible undisclosed side effect by the generic manufacturer’s drug can equate to brand name manufacturer liability for the brand name drug manufacturer’s failure to change the warning label.  This has been coined by some “innovator liability.”

Metoclopramide.jpg

This issue was recently visited by the Judge Higbee in the Superior Court of New Jersey in Coundouris v. Wyeth, et al., No. ATL-L-1940-10 (June 26, 2012) through a motion to dismiss filed by the brand name manufacturers.  The drug at issue there was metoclopramide (the brand name, Reglan, made by Wyeth then Schwarz then Alaven) which is used to treat gastroesophageal reflux disease and diabetic gastroparesis.  Some of the plaintiffs in Coundouris never took Reglan but the generic metoclopramide. The plaintiffs brought claims of conscious misrepresentation, negligent representation, negligence, claims under New Jersey’s Product Liability Act (“PLA”) for design defect and manufacturing defect, and warranty claims.

In their motion to dismiss, the brand name defendants argued that the plaintiffs' claims were governed by the PLA, “and that pursuant to the PLA and New Jersey case law, manufacturers of a brand-name drug may not be held liable for injuries caused by a plaintiff's use of a generic drug manufactured by another company.” In opposition:

Plaintiffs argue that their claims against Brand Defendants are not products liability claims governed by the PLA, but are instead negligence claims governed by New Jersey common law. Plaintiffs contend that the Brand Defendants owed a duty to those ingesting generic metocloprarnide to exercise reasonable care in either disseminating accurate, nonmisleading information about metocloprarnide or adequately warning doctors and patients as to the risk of the drug.

The New Jersey court makes short work of the plaintiffs argument.  First the court holds the plaintiffs’ claims are product liability claims.  Since the plaintiffs’ claims fall under the PLA, Plaintiffs' action must fail because they did not ingest a product made or sold by the brand name defendants. In New Jersey, "it is well-settled that in products-liability litigation, [a plaintiff] must demonstrate that his or her injuries were caused by ... defendant's ... product."

Where Plaintiffs never ingested metoclopramide manufactured or sold by the Brand Defendants, they are unable to establish an essential element of their prima facie case under New Jersey law, and their claims against the Brand Defendants must be dismissed.

In its decision, the New Jersey court quotes a prior New Jersey decision, Rossi v. Hoffman-LaRoche, No. ATL-L-690-05 (January 3, 2007), which dealt with a similar issue of brand name drug manufacturer liability for injuries caused by a generic drug: there is “no evidence” that “the New Jersey legislature intended for prescription drug liability to extend to the name-brand manufacturer when the alleged victim ingested a generic equivalent manufactured and sold by another company."  Thus, in Rossi, as in Coundouris, the court declined to create a duty on the part of the brand name manufacturer to the consumers of a generic drug.

The Boulder Business Lawyers at Laszlo & Associates, LLC provide legal counsel for businesses on a variety of business needs, including products liability, risk management, corporate protection, and legal compliance.  

The Attorney-Client Privilege And Public Relations Firms In Colorado

A recent District of Colorado decision, A.H. ex rel. Hadijah, v. Evenflo, 2012 WL 1957302 (D. Col. May 31, 2012) (A.H. v. Evenflo.pdf), dealt with the issue of whether communications with a public relations firm are privileged under Colorado law.

For the most part, the involvement of a third party to otherwise attorney-client privileged communications destroys the privileged nature of those communications—beit an inadvertent or voluntary disclosure.  However, particularly in the context of high-profile litigation which receives much national attention, defendant companies routinely hire a public relations firm to assist in managing the defendant’s public image in the face of litigation, including assisting in any potential product recall efforts.

The issue of extending the attorney-client privilege to public relations firms and other third party consultants has received much attention over the past decade or so in the various courts of New York. The Southern District of New York court in In Re Copper Market Antitrust Litigation, 200 F.R.D. 213, an often cited case, applied the “functional equivalent” test for PR firms—meaning was the public relations firm the functional equivalent of an employee.  If so, then communications with the public relations firm were privileged.  This same district later took a slightly different approach and looked at who hired the public relations firm—the attorneys or the client—and/or what was the purpose behind hiring the public relations firm.  In In Re Grand Jury Subpoenas, 265 F.Supp.2d 321, the Southern District of New York held that “that (1) confidential communications (2) between lawyers and public relations consultants (3) hired by the lawyers to assist them in dealing with the media in cases such as this (4) that are made for the purpose of giving or receiving advice (5) directed at handling the client's legal problems are protected by the attorney-client privilege.”  (At the link is an interesting article reviewing the various treatments of third party consultants in the state of New York.) 

The District of Colorado had previously adopted the “functional equivalent” test as to “whether to extend the attorney-client privilege to third parties acting at the behest of a client or their attorney”, citing Horton v. U.S., 204 F.R.D. 670 (Colo. 2002). (The Supreme Court of Colorado also did so in Alliance Const. Solutions, Inc. v. Dept. of Corr., 54 P.3d 861. (Colo. 2002))  The Evenflo court cited to the “functional equivalent” test used by the Southern District of New York but it unclear whether this was in fact the test used by the Colorado district court:

(1) “whether the consultant had primary responsibility for a key corporate job,” (2) “whether there was a continuous and close working relationship between the consultant and the company's principals on matters critical to the company's position in litigation,” and (3) “whether the consultant is likely to possess information possessed by no one else at the company.

Turning to the communications at issue in Evenflo, the district court reviewed the nature of Evenflo's interactions with the public relations firm, Zeno Group.  Zeno was hired by Evenflo “to work with its counsel and provide advice regarding the recall/retrofit campaign.” Since Evenflo did not have an internal public relations department, Zeno served as a “functional equivalent” to an internal PR department.  Zeno prepared communications regarding the recall and prepared press releases and communications to the public, incorporating “input from Evenflo's officers, employees and counsel in the proposed communications.”  

According to the Evenflo court, the "...application of the attorney-client privilege [can] be extended to non-employees, however, the party asserting the privilege must make a detailed factual showing that the non-employee is the functional equivalent of an employee and that the information sought from the non-employee would be subject to the attorney-client privilege if he were an employee of the party.” Using this standard, the court found most of the communications to be privileged:

Based on the facts of this case, the Court finds that there is no principled reason to deny attorney-client protection to communications involving employees of Zeno Group with Evenflo's legal counsel that in camera review reveals were primarily or predominately of a legal character and therefore would be considered privileged attorney-client communications if Mr. Armstrong, Mr. Waterman, or Ms. Pellegrino were technically employees of Evenflo. Therefore, this court finds that communications involving the Zeno Group employees are entitled to the same attorney-client protection had the Zeno Group employees actually been Evenflo employees and the privilege has not been waived by their inclusion in several of the protected communications.

That being said, the court however did find that two documents were not protected by the attorney-client privilege—which offers some caution as to how far this “functional equivalent” test will be applied.  The first was an e-mail where no attorney was even included in the transmission.  As the court stated, even if an attorney had been involved with the drafting of the e-mail at some point, the communication did not contain “confidential matters communicated by or to the client in the course of gaining counsel, advice, or direction with respect to the client's rights or obligations.”  Regarding the second item referenced by the court, while the initial e-mail in a string of e-mails was found to be protected by the attorney-client privilege, the subsequent e-mails in the string were not privileged:

However, beyond the original message in the email, the communication merely forwards a series of communications which are not subject to attorney-client privilege. The attorney-client privilege only protects disclosure of communications; it does not protect disclosure of the underlying facts by those who communicated with the attorney.

As the court summed up simply: a party cannot conceal facts subject to discovery merely by revealing them to its lawyer.

The Boulder Business Lawyers at Laszlo & Associates, LLC provide legal counsel for businesses on a variety of business needs, including products liability, risk management, corporate protection, and legal compliance.  

District Court Rejects "Failure-To-Withdrawal" For Generic Drug Manufacturers

We discussed the First Circuit’s opinion in Bartlett v. Mutual Pharmaceutical in two previous posts (here and here). In a nutshell, in Bartlett, the First Circuit refused to find preemption under the Supreme Court’s opinion in Pliva v. Mensing for the plaintiff’s design defect claim against the generic drug manufacturer because the generic manufacturer could “…avoid defective warning lawsuits as well as design defect lawsuits by not making the drug...” in the first place.

Confronted with a similar issue, the District Court for the Eastern District of Kentucky in In Re Darvocet, Darvon, and Propoxyphene Products Liability Litigation MDL reviewed the Bartlett decision and found the First Circuit’s reasoning unconvincing…to say the least. In fact, the district court did not even really offer a review of Bartlett in its opinion at all--that's how unconvinced the Kentucky court found Bartlett.

The plaintiffs in the Darvocet MDL offered the recent Bartlett decision in response to a show cause order as to why claims against certain generic defendants should not be dismissed on Mensing preemption grounds. The district court quickly dismissed the Bartlett reasoning:

Having reviewed the Bartlett decision, the Court agrees with the Generic Defendants.  In Bartlett, the First Circuit adopted the “failure-to-withdraw” argument previously rejected by this Court and others…This argument—which failed to persuade either the Supreme Court or the Eighth Circuit on remand in Mensing, and the Sixth Circuit in Smith v. Wyeth, Inc.—is no more availing now. Moreover, the First Circuit offered little explanation for accepting it, noting simply that the Mensing opinion had not specifically addressed design-defect claims. 

Consequently, the Eastern District of Kentucky court dismissed the claims against the generic drug manufacturer defendants.

Although the district court made summary work of the Bartlett decision, the Eastern District of Kentucky's opinion raises similar points we raised in our second post.  Namely, the “failure-to-withdraw from the market” argument was already rejected by the Supreme Court in Mensing—such rejection was in fact even mentioned by the First Circuit in Bartlett.  Despite recognizing that the argument was already rejected in the context of a failure-to-warn claim, the First Circuit offered no explanation as to why the underlying rationale would not also lead to Mensing preemption for a design defect claim.

The Boulder Business Lawyers at Laszlo & Associates, LLC provide legal counsel for businesses on a variety of business needs, including products liability, risk management, corporate protection, and legal compliance.  

Can a Website be Liable for Promoting an Inherently Dangerous Activity? UPDATED

I am a cyclist and avid Strava.com user (Strava.com allows cyclists to map and clock their times and speeds using GPS and upload them to its website.)  Just this past Sunday, I was on the road in 100 degree heat trying to beat a few of my segment “personal records” – one segment in particular I wanted big time.  I pushed myself, got to the top and thought “I can’t wait to get home, throw this ride on Strava and see hBIKE GPS.jpgow I did.”  Alas, I was off my best time by two seconds … next time.  Strava has motivated me to ride at times when my will power was susceptible to the thought of a cold beer.  However, I have often thought how Strava could (and almost undeniably does) “motivate” cyclists to ride aggressively in order to break records and rank on particular segments created by its members.   

Yesterday, the family of Kim Flint, a cyclist who died when he drifted into the other lane and hit a car while riding his bicycle around a curve brought a lawsuit against Strava, Inc. claiming the popular site was negligent in promoting and encouraging cyclists, like Mr. Flint, to compete on dangerous roads in order to gain standing on the website.

So, what, if any, responsibility does Strava have to its cycling members?  Well, there is the product itself: an online athletic data collection and social networking site.  But the data is based on a member’s activity, in this case cycling – bottom line is you have to cycle to capture data in order to upload data to the site.  So, a necessary component of Strava is cycling.  Strava is so popular because of its "segments" - portions of rides/routes Strava members create and then compete on.  Strava itself does not create these segments.  What Strava does is collect member data and organize and present it on leaderboards for each segment.

In May, 2010, Strava.com's Terms made no mention of associated risks of cycling.  Currently, Strava’s Terms reads as follows:

YOU EXPRESSLY AGREE THAT YOUR ATHLETIC ACTIVITIES, WHICH GENERATE THE CONTENT YOU POST OR SEEK TO POST ON THE SITE (INCLUDING BUT NOT LIMITED TO CYCLING) CARRY CERTAIN INHERENT AND SIGNIFICANT RISKS OF PROPERTY DAMAGE, BODILY INJURY OR DEATH AND THAT YOU VOLUNTARILY ASSUME ALL KNOWN AND UNKNOWN RISKS ASSOCIATED WITH THESE ACTIVITIES EVEN IF CAUSED IN WHOLE OR PART BY THE ACTION, INACTION OR NEGLIGENCE OF STRAVA OR BY THE ACTION, INACTION OR NEGLIGENCE OF OTHERS. YOU ALSO EXPRESSLY AGREE THAT STRAVA DOES NOT ASSUME RESPONSIBILITY FOR THE INSPECTION, SUPERVISION, PREPARATION, OR CONDUCT OF ANY RACE, CONTEST, GROUP RIDE OR EVENT THAT UTILIZES STRAVA’S SITE. www.strava.com June/2012

UPDATED: 6/19/2012 7:16pm Strava emailed its members with the following message:

Posted by  on June 19th, 2012

We’ve updated our terms and conditions, and we’re doing everything we can to get the word out. You’ll also see a notice on your dashboard when you log in to strava.com.

What’s changed? We’ve grown a lot and have expanded our products and services since our terms were last updated. The updated terms clarify things related to our mobile apps, as well as real-world races and events that you might participate in that use Strava’s site.

That short description isn’t meant to be a substitute for the real deal, so please take the time to read the revised terms and conditions found at strava.com/terms. If you use one of our mobile apps, please download the latest version to access the updated terms from inside the app. Then, get back out there and go for a ride or a run.

Thanks,
The team at Strava

But does it matter that Mr. Flint did not expressly agree to assume the risks of cycling when he joined Strava.com?  Probably not.  Mr. Flint was an avid cyclist.  He would have known the associated and inherently dangerous risks of cycling - and more specifically, the risks of cycling at a high rate of speed down a steep grade that is traveled by cars.  Mr. Flint had ridden the particular “segment” before (indeed was riding for the sole purpose of regaining his position as the fastest rider on that segment) and would have known the risks inherent on the ride.

According to Frances Dinkelspiel of Berkeleyside News,  Mr. Flint had raced down South Park Road (the rode on which the collision occurred a few weeks later) on June 6, 2010 in 2 minutes and 7 seconds, reaching a top speed of 49.3 mph.  The speed limit on South Park Drive, which is a steep grade, is 30 miles per hour.  “49.3 mph, on a bike. How I find religion on Sunday morning,” “Set new personal records – Centennial, 3 Bears, some others, even a KOM (King of the Mountain) on south gate descent!” Mr. Flint wrote on June 6.

strava shot.jpg

Under California law, primary assumption of risk arises where an individual voluntarily participates in an activity or sport involving certain inherent risks – in this case, cycling.  Cycling is an inherently dangerous sport.  For example, in order to obtain a cycling license from USA Cycling, a rider is required to sign an “Acknowledgment of risk, release of liability, indemnification agreement and covenant not to sue” which states: “I ACKNOWLEDGE THAT CYCLING IS AN INHERENTLY DANGEROUS SPORT…”

There is no doubt that Mr. Flint’s death is a sad event.  However, Mr. Flint’s death was precisely the type of injury he assumed the risk of encountering while cycling.  There is no question that Mr. Flint voluntarily chose to ride his bicycle - nor that he chose to ride in the manner he did.  It also seems quite clear that he knew of and accepted the risks associated with cycling – Mr. Flint was an avid cyclist, joined a website dedicated to cycling and rode to achieve cycling “records.”  He undoubtedly was aware of the fact that the streets on which he rode, whether “segments” or not, were full of hazards including moving cars.  This, along with what will come out in discovery; Strava should not have to prove much more to establish that Mr. Flint knew of and/or appreciated that a “serious injury” or death could result from his activity.

It is important that companies which promote or involve potentially or inherently dangerous activity be sure their terms of service or user agreements contain adequate warning and release language.  Like many other companies in the heath and fitness arena, Strava is a growing company with increased exposure - and with increased exposure come, well, increased exposure. While I am not sure what kind of legal budget or threshold for litigation the company has, especially in light of the fact it is currently involved in a patent lawsuit, I would look for Strava to vigorously defend this case to set an example for similar claims going forward.

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.

Pennsylvania Supreme Court Rules Plaintiff's Expert Opinion That "Any Exposure" To Asbestos Fiber Is A Substantial Factor In Causing Asbestos-Related Disease Is Inadmissible

The Pennsylvania Supreme Court issued an opinion that, according to one asbestos plaintiffs' blog, "could have far-reaching implications." Betz v. Pneumo Abex LLC was an automotive friction products asbestos case.  The focus of the court’s decision was on the admissibility of plaintiff’s expert opinion that “that each and every exposure to asbestos—no matter how small—contributes substantially to the development of asbestos-related diseases.”  This opinion is often referred to as the "‘any-exposure,’ ‘any-breath,’ or ‘any-fiber’ theory of legal (or substantial-factor) causation.”  This particular case was selected from others below using a similar “any-exposure” theory of causation.  

When determining the admissibility of expert testimony, Pennsylvania still uses the Frye test of “general acceptance in the relevant scientific community applicable to novel scientific evidence” and does not use the Daubert standard.  

First, the Pennsylvania Supreme Court agreed with the court below that the any-exposure theory was novel and thus a Frye hearing was warranted.  In turning to the any-exposure theory of substantial causation, the court noted that the expert’s opinion created an “irreconcilable conflict with itself” because "[s]imply put, one cannot simultaneously maintain that a single fiber among millions is substantially causative, while also conceding that a disease is dose responsive."

In fact, the court quoted the plaintiff’s experts’ own testimony to demonstrate this contradiction:

Now, individual exposures differ in the potency of the fiber to which an individual is exposed, to the concentration or intensity of the fibers to which one is exposed, and to the duration of the exposure to that particular material. So those are the three factors that need to be considered in trying to estimate the relative effects of different exposures. But all exposures have some effect.

To elucidate his opinion that even a single asbestos fiber can be a substantial contributing factor in developing an asbestos-related disease, plaintiff’s expert offered an analogy of a glass of water with marbles being placed into the glass.  In other words, each marble is a substantial factor in the water overflowing.  However, the court found this analogy discomforting, particularly in light of the plaintiff’s expert's previous testimony as to size and potency of asbestos fibers:

In this regard, the analogies offered by [plaintiff’s expert] in support of his position convey that it is fundamentally inconsistent with both science and the governing standard for legal causation. The force of his marbles-in-a-glass illustration changes materially upon the recognition that, to visualize this scenario in terms of even a rough analogy, one must accept that the marbles must be non-uniform in size (as asbestos fibers are in size and potency), microscopic, and million-fold. From this frame of reference, it is very difficult to say that a single one of the smallest of microscopic marbles is a substantial factor in causing a glass of water to overflow.

While this was one of many analogies used by the plaintiff’s expert (also employed: a “soldier in the field” analogy, an “Ellis Island” analogy, a “boxer’s glancing blow” analogy, and a “single cigarette among many” analogy), no analogy offered to the court was found convincing:

We appreciate the difficulties facing plaintiffs in this and similar settings, where they have unquestionably suffered harm on account of a disease having a long latency period and must bear a burden of proving specific causation under prevailing Pennsylvania law which may be insurmountable. Other jurisdictions have considered alternate theories of liability to alleviate the burden. Such theories are not at issue in this case, however, and we do not believe that it is a viable solution to indulge in a fiction that each and every exposure to asbestos, no matter how minimal in relation to other exposures, implicates a fact issue concerning substantial-factor causation in every “direct-evidence” case. The result, in our view, is to subject defendants to full joint-and-several liability for injuries and fatalities in the absence of any reasonably developed scientific reasoning that would support the conclusion that the product sold by the defendant was a substantial factor in causing the harm. 

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.

Sixth Circuit: Defendant Manufacturer Cannot Warn of Unknowable Risk

The title of this post might seem like an obvious statement but it is something worth reviewing from time to time...forest-for-the-trees and all.

Rodriguez v. Stryker Corp. was a recent pain pump decision delivered by the Sixth Circuit.  We previously wrote about another pain pump decision in Pritchett v. I-Flow Corp., involving the use of a “differential diagnosis” to establish general causation.  While also involving issues of causation, the opinion in Rodriguez also dealt with whether it was possible for Stryker to reasonably know that its pain pump could have caused the injury complained of in 2004.

In November 2004, the plaintiff, Andrew Rodriguez, had shoulder surgery in which a pain pump was implanted.  Through the pain pimp, the plaintiff received a local anesthetic, bupivacaine, to the shoulder joint.  While the plaintiff initially improved, his condition worsened until he discovered in 2008 that he longer had any cartilage in his shoulder—a condition called chondrolysis.  The plaintiff filed suit in 2008 alleging negligence, strict liability, and breach of warranty.  The district court concluded that Stryker could not have reasonably known in 2004 of the risk of pain pumps causing chondrolysis and thus Stryker had no duty to warn of what was unknowable at the time.

The Sixth Circuit began its inquiry by noting that under Tennessee law (similar to many states) a manufacturer must warn of known risks caused by its products or risks that should have been known through exercising reasonable care.  The court quickly determined, and the plaintiff did even attempt to claim to the contrary, that it was impossible for Stryker to know in 2004 that anesthetics injected by its pain pump could cause chodrolysis—“no reported case of chondrolysis linked to anesthetics appears until 2005.”  So the only way for the plaintiff to show that Stryker had a duty to warn was to establish that Stryker should have known of the chondrolysis risk.

Which brings us to the thirteen published articles submitted by plaintiff.  According to the court, 

none of the articles draws a connection between pain pumps and chondrolysis, leaving Rodriguez to argue something more inferential:  that the studies “document[ ] significant damage to articular cartilage after prolonged exposure to foreign solutions, including bupivacaine”….Even that is a stretch, however, given what the articles say.

After reviewing each article, the court determined: “[w]hen all is said and done, not one of Rodriguez’s thirteen articles shows that medical experts understood in 2004 that infusing a joint with bupivicaine for two days could cause irreversible cartilage damage.”  For this reason, “Stryker had no duty to understand what the relevant medical literature did not.”

Turning to the expert report, the court was similarly unconvinced that it provided evidence that Stryker had a duty to warn about chondrolysis in 2004.  According to the court, the plaintiff's expert report claimed that “general medical knowledge about articular cartilage, combined with the then-extant scientific literature, should have put Stryker on notice that this pain pump would harm cartilage.”  After stating the proposition that a court has a duty to inspect the reasoning of an expert, “including whether an expert’s sources support his conclusions,” the Sixth Circuit found the latter requirement lacking in the plaintiff’s expert report:

[The expert] relies on several articles published after Rodriguez’s surgery, which do not speak to what Stryker should have known months or years earlier based on expert knowledge at the time.  He also relies on articles published before Rodriguez’s surgery, but they are the same thirteen articles discussed above, and none of them supports the conclusion that Stryker reasonably should have known about the risk that its pumps could cause chondrolysis.  The thirteen articles, indeed, undermine the expert report because they show that medical experts did not understand the risks posed to cartilage by pain pumps in 2004, when Rodriguez had his surgery.

Neither the thirteen articles nor the expert report submitted by the plaintiff demonstrated that Stryker had a duty in 2004 to warn of the risk of chondrolysis.  Stacking inference upon inference does not establish a duty-to-warn.  Moreover, the district court need not have submitted this case to a jury “containing only a spark or glimmer of evidence that requires the finder-of-fact to make a leap of faith to find the defendant liable for the plaintiff’s injury.” Thus, the court held that the plaintiff failed to establish that Stryker had a duty to warn of the risk of chondrolysis caused by its pain pumps in 2004:

That is just the problem here.  Rodriguez asks a jury to find that because there were isolated instances over seventy years when evidence showed that a few foreign solutions caused temporary harm to joint cartilage, Stryker should have known (and warned) that using its pain pump in a joint with bupivicaine would cause permanent damage.  On this record, the theory requires two speculative leaps.  It requires the inference that evidence of harm resulting from other solutions meant that anesthetics would cause the same harm.  And it requires the inference that evidence of transient harm to joints meant that irreversible cartilage damage was likely.  Both are far too conjectural and too many steps removed from the problem that developed.  Just because ingesting one type of liquid over a period of time may cause a problem does not mean that ingesting another liquid will cause the same problem.  And just because cleaning a wound with rubbing alcohol causes temporary discomfort does not permit the inference that cleaning a wound more than once will produce permanent discomfort.  To conclude otherwise would establish a claim for hindsight negligence, not common law negligence.

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.

District Court of Colorado: Expert Opinions Based On "Differential Diagnosis" Can Show General Causation

Pritchett v. I-Flow Corporation, Inc. is a recent pain pump case in front of the United States District Court of Colorado.  The plaintiff had shoulder surgery in 2005.  The surgeon used a pain pump manufactured by I-Flow to inject an anesthetic into the shoulder joint over a 48 hour period which allegedly led to the development of “chondrolysis”—a partial or complete loss of cartilage in the shoulder joint.  Plaintiff alleged that the pain pump was marketed by the defendant I-Flow “without doing a single study to determine whether pain pump anesthetics could harm cartilage.”  Additionally, the plaintiff claimed that I-Flow waited years to inform physicians after receiving notice that its pain pump could damage cartilage.

The issue in the April 17, 2012 decision surrounded the defendant’s attempts at excluding the plaintiff’s expert witness, Dr. Jon Hyman.  Among other reasons for excluding the plaintiff’s witness, the defendant argued that Dr. Hyman’s “differential diagnosis of specific causation is invalid in light of the lack of evidence of general causation and because Dr. Hyman failed to rule out other potential causes of Plaintiff's shoulder injury.”  A differential diagnosis is generally the determination of which one of several diseases may be producing the symptoms experienced by a patient.

After reviewing Fed. R. Evid. 702's analysis and application generally, the court, in a rather conclusory fashion, determined that the Dr. Hyman's opinions were admissible.  According to the court, quoting a prior pain pump case McClellan v. I-Flow Corp., “taking [I-Flow's] argument to its logical conclusion, [I-Flow] would have [Plaintiff] prove causation to a medical certainty before expert testimony could be admitted.“  The court found this “wholly inconsistent with Daubert and the fundamental premise of Rule 702.”  Moreover, again quoting from McClellan:

Daubert did not impose an exacting standard of causality beyond the preponderance of the evidence simply because scientific issues are involved…The issue is not whether the proponent of expert testimony can prove that the expert is correct; it is whether the testimony is reliably derived from scientific methodology and is relevant to the facts of the case.

According to the court, Dr. Hyman’s use of a differential diagnosis did not “doom” his opinions under Daubert since “numerous courts have approved opinions based on differential diagnosis to show general causation, despite the absence of conclusive causal evidence.” (emphasis added).

As stated above, the court’s support for its conclusion is not rigorously grappled with: “[g]enerally ‘the basis for establishing the scientific validity of a differential diagnosis will vary depending on the type of injury and whether it involves a complicated biological explanation, a long latency period or the lack of a single sharp exposure event.’” For this reason, despite the fact that Dr. Hyman used a differential diagnosis in his opinion of the plaintiff’s condition:

Case-specific factors, such as the temporal relationship between the continuous infusion and Plaintiff's development of chondrolysis, Plaintiff's lack of other toxic exposures, and Plaintiff's lack of other systemic disease or injury unrelated to the area or purpose of exposure, increase the reliability of the differential diagnosis methodology used here.  In these circumstances, Dr. Hyman's testimony on general causation should be admitted because it is based on a reliable differential diagnosis and reliably flows from the underlying facts of the case.

The court was not overly concerned that Dr. Hyman’s opinion may attribute a different cause for the plaintiff’s condition to say the least.  Moreover, the court, in what justification it did offer, seemed to be convinced that the lack of “complexity” as to the nature of the plaintiff’s injury provided an acceptable basis for summarily allowing a differential diagnosis to support general causation.

The Boulder business lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.

Is Your Company Prepared For a Recall? If You're Not On Twitter, You're Not Prepared.

Cervelo Wolf Fork.jpg

 

In 2003, Cervelo, the maker of high end road bicycles, voluntarily, and in conjunction with the U.S. Consumer Product Safety Commission, recalled 317 Wolf all carbon road bicycle forks.  In April 2012, a Massachusetts man riding on a bike fitted with the recalled forks crashed and died.  Police stated that the rider was on a Cervelo Soloist and that it appeared a "mechanical failure" causing the forks to separate from the bike led to the crash.  An investigation is currently underway, but let us assume, for purposes of this article, that the recalled Cervelo forks caused the accident and ultimately the man’s death.

Most punitive damage awards stem from evidence that the manufacturer knew or should have known about a post-sale problem but failed to take adequate remedial measures to prevent accidents.

In the Cervelo case, the recalled Cervelo forks were sold from April 2003 until July 2003 - with a recall announced July 31, 2003.  It would appear that Cervelo worked swiftly to recall the defective forks.  But with only 300 forks sold in such a short period of time, how was it that Cervelo was unable to reach all owners of the forks?  The bottom line is no one should have been riding on those forks.  In its latest Consumer Product Safety Commission Recall Handbook, the CPSC lists dozens of ways to inform consumers of a product hazard and recall.  Of note is the social media aspect, perhaps the most efficient way to reach your consumer:

The Commission encourages companies to be creative in developing ways to reach owners of recalled products and motivate them to respond ... As new or innovative methods of notice and means of communication become available, such as social media, the staff encourages their use. ...  use of a firm’s social media presence to notify consumers of the recall, including Facebook, Google +, YouTube, Twitter, Flickr, Pinterest, company blogger networks, and blog announcements.

Just this week, bike manufacturer Specialized issued a recall due to hazardous break levers. However, the company has not yet announced the recall on Twitter - where it has more than 60,000 followers.  Others have tweeted about the recall but nothing from the Specialized company itself (as of the writing of this blog post). This is such a missed opportunity - Specialized can immediately reach 60,000+ consumers who will immediately get the information it provides (not to mention there are more likely than not some affected consumers following on Twitter.)

In the Cervelo case, a question will certainly be asked whether Cervelo did everything it reasonably could have done to ensure all forks were replaced.  How did (if at all) Cervelo try to inform the man that his bike was one that had the defective forks? Twitter was not around in 2003, and it is doubtful the company had policies and procedures in place to notify customers via social media at that point. But times have changed.  It is 2012, and there is simply no excuse not to use social media to inform consumers of hazards and recalls associated with your products.  And keep in mind that many (if not most) of your jurors will use and understand Twitter, Facebook and the latest social media - and wonder why you did not use it to let them know they could get hurt.

The Boulder lawyers at Laszlo & Associates, LLC provide legal counsel to businesses on a variety of business needs including products liability, risk management, corporate protection and legal compliance.

 

Nice Marmet: Another Victory for Arbitration in the Supreme Court of the United States - State's Public Policy Doesn't Trump the FAA.

United_states_supreme_court_building.pngLast month, the Supreme Court of the United States overturned a West Virginia Supreme Court’s ruling that the Federal Arbitration Act (FAA) does not pre-empt the state public policy against predispute arbitration agreements that apply to claims of personal injury or wrongful death against nursing homes.

In Marmet Health Care Center, Inc. v. Brown, (three similar cases were consolidated before the W.Va. Supreme Court) family members of patients requiring ex­tensive nursing care had signed agreements with the nursing homes that required the parties to arbitrate all disputes for personal injury or wrongful death.

The West Virginia Supreme Court held that such “predispute” arbitration agreements were against West Virginia public policy and therefore unenforceable.

In a decision concerning all three cases, the state court held that “as a matter of public policy under West Virginia law, an arbitration clause in a nursing home admission agreement adopted prior to an occurrence of negligence that results in a personal injury or wrongful death, shall not be enforced to compel arbitration of a dispute concern­ing the negligence.” Brown v. Genesis Healthcare Corp. (Citations omitted).

The West Virginia Supreme Court also concluded that the state's public policy against such predispute arbitration agreements, as they apply to personal injury and wrongful death claims, was not pre-empted by the FAA.

The Supreme Court of the United States held that the “West Virginia court’s interpretation of the FAA was both incorrect and inconsistent with clear instruction in the precedents of this Court.”

The FAA provides that a “written provision in . . . a contract evidencing a transac­tion involving commerce to settle by arbitration a contro­versy thereafter arising out of such contract or transaction. . . shall be valid, irrevocable, and enforceable, save upon such grounds as exist at law or in equity for the revocation of any contract.”  The statute’s text includes no exception for personal-injury or wrongful-death claims. … As this Court reaffirmed last Term, “[w]hen state law prohibits outright the arbitration of a particular type of claim, the analysis is straightforward: The conflicting rule is displaced by the FAA.” AT&T Mobility LLC v. Concep­cion.  That rule resolves these cases.  (Citations omitted).

The take away from the Marmet and the AT&T Mobility cases is that a state’s prohibition against predispute agreements - even those predicated on public policy - to arbitrate particular types of claims are indeed categorical rules prohibiting arbitration of a particular type of claim, and thus contrary to the terms and coverage of the FAA. 

Sixth Circuit Overturns Asbestos Verdict Because Plaintiffs Failed to Prove Exposure Was a "Substantial Factor" in Causing Mesothelioma

In Moeller v. Garlock Sealing Technologies, LLC, (6th Cir. Sept. 28, 2011), the Circuit court decided whether evidence presented by a Plaintiff regarding exposure to asbestos was sufficient to support a determination that the manufacturer's asbestos-containing gaskets were a substantial factor in bringing about the pipefitter's injuries and death.  The court held the evidence was insufficient.   In Moeller, Mr. Moeller, a pipefitter, worked with asbestos insulation from 1962 through 1975.  During the same period, Plaintiff worked with Garlock gaskets which contained asbestos.  Mr. Moeller died from mesothelioma in 2008, his widow sued numerous defendants including Garlock.  Under Kentucky state law, to prevail on a negligence claim, a plaintiff must prove that a defendant’s conduct was a substantial factor in bringing about the harm.  At trial, with respect to causation, Plaintiff presented the testimony of a doctor of internal medicine who opined that Plaintiff’s exposure to asbestos from Garlock gaskets, along with other exposures, contributed to Robert’s mesothelioma. 

The jury returned a verdict for Plaintiff in the amount of $516,094.  Defendant Garlock moved for judgment as a matter of law and for a new trial – both motions were denied.    Here, because Plaintiff’s experts admittedly never testified that Plaintiff’s exposure to Garlock gaskets was a substantial factor in causing his mesothelioma, the Sixth Circuit held that Plaintiff was unable to establish that exposure to Garlock gaskets in and of itself was a substantial factor in causing the mesothelioma.  Therefore, under Kentucky law, Plaintiff failed to prove her case and Garlock’s motion for judgment as a matter of law should not have been denied. 

This case reaffirms the recent theme the importance of good and thorough expert testimony.  Here, Plaintiff’s experts did not, as they were likely unable, to opine that Garlock’s gaskets were a substantial factor in causing Mr. Moeller’s mesothelioma.  With such evidence being so critical to the claim however, plaintiff’s counsel should have developed additional or alternative evidence regarding causation.    

When Experts are Required and What is Required of Experts: Three Recent Opinions

Three recent opinions involved interesting and important issues regarding experts – Show v. Ford Motor Co., (7th Cir. Sept. 19, 2011), Anderson v. Akzo Nobel Coatings, Inc. Supreme Court of Washington (Sept. 8, 2011), and Bertrand v. Gen. Elec. Co., (US Dist. Mass. Sept. 21, 2011).

In Show v. Ford Motor Co., (7th Cir. Sept. 19, 2011), the Circuit Court affirmed the USDC Illinois court’s grant of summary judgment in favor of Ford Motor Company based on the fact that in their product liability action against Ford Motor Company, plaintiffs had not designated an expert on the subject of defective design.  Plaintiffs’ position was that jurors, as consumers, can find in their own experience all of the evidence required for liability under the consumer expectation test and therefore, an expert on the subject was unnecessary.  Ford disagreed.  Both Parties and the magistrate judge agreed that state substantive law controlled the issue of whether expert testimony was necessary a position the 7th Circuit ultimately affirmed.  Interestingly however, was the Circuit Court’s persistence in mentioning the question of whether Federal or State law actually controlled the issue had the parties not agreed to state law.

Whether or not this implies that federal law determines what kind of evidence is required-a subject that we bypass, given the parties’ shared assumption…”  “…once again we bypass the question of whether state or federal law governs the methods of proof in federal court.

In Anderson, the plaintiff offered expert testimony to support her position that that exposure to organic solvent while pregnant resulted in brain damage to her child.  The defendant challenged the expert’s theories and methods as novel and not generally accepted in the scientific community.  In Anderson, as in Show, because both the parties and the lower courts agreed on what law controlled, i.e., that the Frye test was appropriate, the Washington Supreme Court declined to decide whether Frye was actually the appropriate test for civil cases. 

The Washington Supreme court held “the Frye test is only implicated where the opinion offered is based upon novel science … Frye does not require every deduction drawn from generally accepted theories to be generally accepted …because Dr. Khattak’s testimony was not based upon novel science, Frye was not implicated in this case.”  The Court stated specifically:

In civil cases, we have neither expressly adopted Frye nor expressly rejected Daubert.  In the case before us, the parties and lower courts assume that Frye is applicable, and for purposes of this opinion, we will assume without deciding that Frye is the appropriate test for civil cases.

Finally, in Bertrand v. Gen. Elec. Co., (US Dist. Mass. Sept. 21, 2011), Defendant GE moved to preclude plaintiffs’ expert on a purported lack of qualifications and on Daubert grounds.  Plaintiffs’ expert opined that a defectively-designed stove ignition switch caused the “push-to-turn” safety feature of the burner control valve to fail, permitting a family pet to activate a burner of the stove.  GE argued that plaintiffs failed to demonstrate that their expert, an “all-purpose engineer” was qualified to offer opinions on stove design, and had failed to opine with the requisite degree of reasonable scientific certainty and therefore failed the Daubert test.

Daubert neither requires nor empowers trial courts to determine which of several competing theories has the best provenance. It demands only that the proponent of the evidence show that the expert's conclusion has been arrived at in a scientifically sound and methodologically reliable fashion.”

The Massachusetts district court was satisfied with Plaintiffs’ expert’s qualifications: "A licensed mechanical engineer with an advanced degree and years of hands-on experience with jet engine design and structural analysis ... is well within his competence in examining the workings of a burner switch on a simple kitchen stove."

The court noted that GE's objection to plaintiffs' expert appears based less on any real question about his qualifications than a distaste for the fact that he makes his living as a hired expert in plaintiff's cases. "If the fact of Chen's employment has allowed a bias to creep into his opining, that is a fair subject for cross-examination, but it is not grounds for excluding his testimony altogether."

Show, Anderson and Bertrand, while different, are important to consider for a few reasons.  It appears that the Court of Appeals for the Seventh Circuit is ready and waiting to examine the issue of when state or federal law controls the necessity of expert testimony.  Further, the Washington Supreme Court made clear that it has yet, but appears willing and ready, to decide whether Frye or Daubertis the appropriate test in civil cases. Finally, both Anderson and Bertrand illustrate that it is critical, under Frye and Daubert, to establish that the methodiology employed by your expert is sound and reliable.

Supreme Court Wal-Mart Class Action Decision - Commonality is King

The Supreme Court's recent decision in the Wal-Mart sex-descrimination suit demonstrates the importance of 'commonality' in class actions.  Not to mention that the decision is a good example of why MDLs, free from such 'roadblocks', are the new class actions.  Because MDLs are not regulated in the way class actions are, such a review for lack of commonality reasonably would never occur.

The plaintiffs' case against Wal-Mart was based on an alleged pattern of descrimination in the form of paying women workers less than thier male counterparts and providing them fewer opportunities.  In the end, the allegations were not enough to permit the three named plaintiffs to represent a class of 1.6 million.

Merely showing that Wal-Mart's policy of descrimination has produced an overall sex-based disparity does not suffice. - Justice Scalia. 

 

The "Sunshine In Litigation Act of 2011" May Shed Too Much Light Into The Discovery Process

There has been a lot of rumbling over Senate Bill 623 aka the “Sunshine in Litigation Act of 2011” lately.  Perhaps for good reason.  S. 623 provides in part that:

In any civil action in which the pleadings state facts that are relevant to the protection of public health or safety, a court shall not enter, by stipulation or otherwise, an order otherwise authorized under rule 26(c) of the Federal Rules of Civil Procedure restricting the disclosure of information obtained through discovery, an order approving a settlement agreement that would restrict the disclosure of such information, or an order restricting access to court records unless in connection with such order the court has first made independent findings of fact that--

‘(A) such order would not restrict the disclosure of information which is relevant to the protection of public health or safety; or

‘(B)(i) the public interest in the disclosure of past, present, or potential health or safety hazards is outweighed by a specific and substantial interest in maintaining the confidentiality of the information or records in question; and

‘(ii) the requested order is no broader than necessary to protect the confidentiality interest asserted.

It is certainly understandable why attorneys on either side of the v. would react strongly to S. 623.  Defendants certainly want to protect and direct litigation through discovery strategy.  Such tactics are necessary and effective.  Plaintiffs clearly would benefit from a defendant's fear that a scorched earth discovery effort could uncover damaging documents and that, those facts, if made public, would be highly detrimental to the business. 

S. 623 may be vunerable to loose interpretation resulting in unintended consequnses that inflict considerable damage to parties unable to protect information.  Yet, a middle ground has to be found on this issue.  Bringing a lawsuit cannot be made to give a plaintiff carte blanche to discover and make public anything it wants.  Likewise, a defendant should not be able to hide every single piece of information from public view – especially where public safety may be at issue.  

Further permitting parties to litigate behind closed doors will only hurt our legal system by depriving it of insight, analysis and precedent.  When issues are so intertwined with "confidential facts" that cannot be publicly disclosed, any court order or opinion will necessarily be sealed and will therefore be hidden, likely into perpetuity.  This no doubt will lead to inconsistent rulings, interpretation of laws and results.  Such a reality is a bad result for everyone. 

If A Wine Bottle Breaks While Opening, Is There A Product Liability Claim?

While opening a bottle of wine recently, I struggled with a cork that was just plain stuck.  After some serious effort with the Pulltap, Ah-So and just short of using my 9 iron, I got the thing open.  But not without the thought of what might have been had the bottle burst and glass went flying.  Who would be to blame? Not me of course...but who? The winery? The bottle maker?  The cork supplier?  Turns out, in all likelihood, it would have been my fault.  

In Rabon-Willimack v. Robert Mondavi Corp. a bartender injured her hand after breaking a bottle of Robert Mondavi Woodbridge while opening the wine.  The bartender alleged causes of action sounding in strict products liability, breach of warranty and negligence.  In the end, the bartender could not prove her case as the Defendants successfully argued that there was no manufacturing defect and no flaw in the design as the “bottle fractured due to excessive force applied to the top of the bottle with a two-pronged fulcrum of a waiter’s metal corkscrew.”  Nor was the court persuaded that Robert Mondavi had a duty to warn of the risks created by the use or misuse of another manufacturer’s products or of the danger of applying pressure to a glass bottle with a mental object while holding the bottle in one’s hands.  The court concluded that the expert's opinions were nothing more than specultaion:

As the expert's opinion was not supported by foundational facts, such as the results of actual testing of the bottle, a deviation from industry standards, or statistics showing the frequency of consumer complaints or injuries resulting from the alleged product defect, it lacked sufficient probative value to raise a triable issue of fact as to whether the subject bottle was not reasonably safe in its design.  Rabon-Willimack v. Robert Mondavi Corp., 73 A.D.3d 1007, 1009, 905 N.Y.S.2d 190, 193 (N.Y. App. Div. 2010).

So, be careful when opening your wine, but more important, be extra careful when choosing your expert. 

Michigan Federal Court Dismisses Multiple Plaintiff Action For Failure To State A Claim

Pleading standards issues seem to be all around us these days.  Most recently, the Western District of Michigan took up the issue.  In Abnet, et al. v. Coca-Cola, Co., a case involving many plaintiffs alleging property damage due to groundwater toxicity from a nearby Coca-Cola plant, the court held that the plaintiffs failed to connect the generalized allegations in their complaint with any specific harms to many individual plaintiffs - several plaintiffs did not allege any specific individual harm.  The court further stated:

each individual Plaintiff is obligated to state how Defendants' alleged behavior gives him or her in particular a right to relief.

You can read the full OPINION here.  While specific to the plainitffs that failed to allege any specific individual harm, the Abnet opinion is worth reading as a reminder of the pleading standards under Federal Rule 8.

11th Circuit Overturns Class Certification In YoPlusYougurt Case.

In keeping with our discussion on class certifications (see below), of note is the recent decision of the 11th Circuit vacating an order certifying a class this past Friday.  In Fitzpatrick v. Gen. Mills, Inc., the class consisted of consumers who purchased YoPlus yogurt.  The products liability case alleged that General Mills violated the Florida Deceptive and Unfair Trade Practices Act (FDUTPA) by making false and misleading claims about the digestive health benefits of its YoPlus yogurt.  The District Court certified the class and held that recovery under FDUTPA does not hinge on whether a particular plaintiff actually relied on General Mills' claims about YoPlus' alleged health benefits, but rather, whether the deceptive conduct would deceive an objective reasonable consumer.

The District court concluded its order by defining the class as "all persons who purchased YoPlus in the State of Florida to obtain its claimed digestive health benefit."  Noticeably perplexed by the District court, the 11th Circuit concluded the definition of the class certified was in conflict with the District Court's sound analysis and threw into question what class it actually intended to certify.

The 11th Circuit stated simply that "the district court's analysis in its Order on Motion for Class Certification is sound and in accord with federal and state law. The reasoning reflected therein is well within the parameters of Rule 23's requirements for certification of a class. And, if the definition of the class had been in accord with the legal analysis, we would have readily affirmed." Fitzpatrick v. Gen. Mills, Inc., 10-11064, 2011 WL 1103005 (11th Cir. Mar. 25, 2011). 

While this products liability case appears to revolve around a technicality, it is important to consider the distinction here between the District court's analysis grounded in one definition of the would-be class and the conclusion that greatly limited the class by contradicting its own analysis.  It seems a foregone conclusion that the District court will simply redefine the class in accordance with its analysis and the 11th Circuit's guidance.

Tougher Class Action Certification Equals More MDLs

In the March 2011 edition of DRI's "For The Defense" Michael McCutcheon and Kyle Richard Olson detail and discuss plaintiffs' evidentiary burden of proof at the class certification stage.  The authors state that recent federal court rulings suggest that courts are "willing to engage in a full Daubert inquiry at the class certification stage to determine the admissibility of expert testimony under certain circumstances."  The article is a discussion on which standard of proof applies to Fed. R. Civ. P. 23's class certification requirements.  I believe the article is a good starting point to discuss the effects of rigorous class certification standards on the growing number of MDLs. 

The reality is that as class certification becomes more difficult for plaintiffs - aka "plaintiffs attorneys," the unregulated wild west of Multi-district Litigation becomes much more appealing.  There is no Rule 23 or other certification process in an MDL. 

The emerging burden of proof rule at the certification stage has generally favored defendants.  Plaintiffs’ attorneys hoping for class certification cannot throw bare pleadings against the wall and expect them to stick.

In MDLs, plaintiffs can throw bare pleadings against the wall ... it could be years before an MDL court hears dispositive motions.  The formation of an MDL simply depends on whether the Judicial Panel on Multidistrict Litigation (JPML) believes consolidation will aid in the administration of a given group of cases.  The determination, unlike a class action, is not merit based.  While MDLs can be beneficial to defendants, i.e., consolidating many similar actions around the nation into a single proceeding, MDLs, when formed early, can be an albatross for many years. 

The benefit of an MDL to plaintiffs’ attorneys is the unregulated and lucrative “common benefit fee.”  Common benefit fees are often in the tens of millions (the Toyota MDL fees were anticipated to be in the high hundreds of millions) and are split between a few select lawyers.  Often, the common benefit fund is funded in part directly by the defendant - not just a percentage of the recovery.  Furthermore, MDL judges have unfettered discretion to grant common benefit fees as they wish - often adding arbitrary "multipliers" to common benefit awards.  What this means is that MDLs can be far more attractive than class actions to plaintiffs' attorneys. 

While Messrs. McCutcheon’s and Olson’s analysis on Rule 23 class certification is insightful, it also provides an example of why MDLs are on the rise.  The reality is that class actions are less desirable and potentially less profitable as MDLs have come to be.  Therefore, it may be wise to take a cautioned approach to certification because as class actions become increasingly more difficult to certify, so does the unregulated MDL monster grow.

Supreme Court Rules 'Statistically Insignificant Information' Can Still Be 'Material Information'

On Tuesday, The Supreme Court Ruled 9-0 in favor of the investors in Matrixx Initiatives v. Siracusano (09-1156), March 22, 2011. 

We all may remember well the countless television and radio advertisements for Zicam cold remedy.  But when reports began to surface that some users of the Zicam cold remedy (now a discontinued product) had lost their sense of smell, the manufacturer, Matrixx Initiatives, Inc., saw shares of its stock lose value. In an effort to stem the tide of negative publicity, Matrixx issued statements defending its popular cold medicine by first dismissing the incidence of the loss of sense of smell as exceedingly rare and then taking the additional bold step of proclaiming that there was no scientific basis for linking Zicam to the complained of side effect.

Investors brought class action against Matrixx Initiatives and three of its executives, alleging that they violated federal securities laws by failing to disclose material information about Zicam.  The investors had learned that Matrixx had, on a handful of occasions, been contacted by the medical community regarding the link between the use of Zicam and the loss of smell.  Further, Matrixx made statements about product sales and growth without disclosing that the company had been sued upon claims of loss of smell resulting from the use of Zicam.

The Supreme Court was faced with the question of whether a plaintiff can state a claim for securities fraud under § 10(b) of the Securities Exchange Act of 1934, and Securities and Exchange Commission (SEC) Rule 10b-5, based on a Matrixx’s failure to disclose reports of adverse events associated with its product Zicam if the reports do not disclose a statistically significant number of adverse events.

The Supreme Court held that information regarding a side effect of a drug, even if the side effect is extremely rare, was ‘material information’ upon which a ‘reasonable investor’ may have acted.  The decision now clears the way for the investor class-action lawsuit to move forward against Matrixx, holding that the company had an obligation to reveal details of the observed side effects to investors even though the Company claimed the information did not rise to the level of statistically significant data.

A lack of statistically significant data does not mean that medical experts have no reliable basis for inferring a causal link between a drug and adverse events ... We note that courts frequently permit expert testimony on causation based on evidence other than statistical significance.

Given that medical professionals and regulators act on the basis of evidence of causation that is not statistically significant, it stands to reason that in certain cases reasonable investors would as well.

What is important to recognize here is that Martixx made affirmative statements denying the association between Zicam and loss of smell and omitted certain facts and information relating to those side effects.  Simply, Matrixx was not required to provide the information it had.  However, once Matrixx made satements and representations regarding Zicam, those statements needed to be complete and accurate.

...it bears emphasis that § 10(b) and Rule 10b-5(b) do not create an affirmative duty to disclose any and all material information. Disclosure is required under these provisions only when necessary “to make ... statements made, in the light of the circumstances under which they were made, not misleading.

The Court reasoned that there is no bright line rule requiring statistically significant information embracing, rather, a “total mix” standard of whether a reasonable investor would have viewed the non-disclosed information as significantly altering the total mix of information available to the investing public.

The question remains whether a reasonable investor would have viewed the nondisclosed information ‘as having significantly altered the “total mix” of information made available.’

... the mere existence of reports of adverse events-which says nothing in and of itself about whether the drug is causing the adverse events-will not satisfy this standard. Something more is needed, but that something more is not limited to statistical significance and can come from “the source, content, and context of the reports...

The Court's analysis in Matrixx is important to consider when deciding what information your company should make public.  As is so often the case, the mouth piece of the company may not be aware of certain facts or information which may cause their statements to be "misleading."  Good corporate policy regarding dissemination of information to the public and a clear understanding of that policy is critical.

The Reasonable Expectations Doctrine May Save the Day in Some Situations, But Careful Drafting and an Understanding of the Law is Still Key.

            Most cases involving the reasonable expectations doctrine arise in one or more of three basic contexts: (1) ambiguity in the terms of a policy, either generally or within the framework of a policy exclusion; (2) policy exclusions that undermine the insured's reasonable expectations of coverage; and (3) situations where, by virtue of the policy being a contract of adhesion, the insurer in essence took advantage of the insured by issuing a policy that was not consistent with the insurer's reasonable expectations of coverage.  

            Currently before the Supreme Court of Ohio is the question of whether Ohio law encompasses the reasonable expectations doctrine. 

            In Honeybaked Foods, Inc. v. Affiliated Insurance Co., pending in the United States District Court for the Northern District of Ohio, the case will turn on this very question.  In that case, a risk report completed by Affiliated Insurance prior to Honeybaked purchasing the insurance policy in question noted that “[t]he most significant and common hazards exposing the food industry are centered on the susceptibility of food products to spoilage and contamination.”  Honeybaked purchased the policy mindful of the risk assessment. 

            In early November, 2006, HoneyBaked discovered that a sample of its products had tested positive for listeria monocytogenes, a pathogenic bacterium that causes listeriosis, an uncommon but potentially fatal disease.  Further investigation revealed that a risk of contamination affected over one million pounds of product produced from September 5 through November 5, 2006.  Honeybaked suspended operations and recalled tons of contaminated product.

The Affiliated insurance policy contained a contamination exclusion, stating:

"This policy does not insure against loss or damages caused by [contamination, including but not limited to pollution]; however, if direct physical loss or damage insured by this policy results, then that resulting direct physical loss or damage is covered."

Affiliated denied the claim, explaining that the policy excluded the product loss, and because “there is no covered physical loss or damage, any business interruption associated with the listeria contamination is also not covered.”  Honeybaked sued.

            The trial court stated that “a jury could find that HoneyBaked had a reasonable expectation of coverage for losses due to contamination. But the policy, when closely interpreted, excludes losses caused by contamination.  The availability of coverage, notwithstanding the exclusion, turns on the question of whether Ohio law incorporates the reasonable-expectations doctrine and applies such doctrine to this case.”

            A recent Minnesota decision stated that “The doctrine of reasonable expectations does not destroy the insured's obligation to read the policy, but only holds an insured to a reasonable understanding of that policy.” Frey v. United Services Auto. Ass'n, (Minn. Ct. App. 2008).

            Some states allow for use of the doctrine only under certain circumstances while others are less strict on application.  The Reasonable Expectations Doctrine is a "principle [that] pertains to alleged ambiguities within the policy."   Brown v. Indiana Insurance Co., (Ky. Supreme Court, Dec., 2005.)  "Under Arizona law, even unambiguous policy language will not be enforced against the insured if the insured had a reasonable expectation of coverage."   Madsen v. Fortis Benefits Ins. Co., (U.S.D.C. Ariz., Dec. 21, 2006).

            In Honeybaked Goods, the policy excludes losses from contamination. The risk of such loss, a jury could find, motivated HoneyBaked’s purchase of the Affiliated policy, and that Affiliated knew of HoneyBaked’s desire and need for coverage against losses from contamination.  The court stated: “Whether coverage is available in this case depends on whether Ohio law encompasses the reasonable-expectations doctrine.” 

            The Ohio Supreme Court a is very conservative court, but in a recent decision overturned lower courts and extended coverage to victims of a bus crash finding that where a University had hired a bus driver, the bus driver was covered under the University’s policy.  Fed. Ins. Co. v. Executive Coach Luxury Travel, Inc., (Ohio S.Ct., Dec. 28, 2010.)  What is worth noting is that the Dissent in Fed. Ins. Strongly supports the view that intent of the parties is the critical inquiry in such coverage disputes:

“The majority’s narrow interpretation expands the scope of coverage beyond what the parties to the insurance policy intended,” Justice Stratton wrote. “Today’s opinion unreasonably extends coverage to a third party and effectively opens the door for similar claims under other scenarios because the omnibus clause is standard in many insurance policies.”  Fed. Ins. Co. v. Executive Coach Luxury Travel, Inc., 2010-Ohio-6300 Dec. 28, 2010, Stratton, J. and O'Donnel, J. Dissenting.

            In order for Honeybaked to prevail, The Ohio supreme court will have to rule that Ohio either does or does not recognize the reasonable expectations doctrine and the trial court would have to take an Arizona approach and enforce the policy against the insurer based on the position that Honeybaked had a reasonable expectation of coverage despite the exclusionary language. 

            What is the lesson here?  Despite the availability of the reasonable expectations doctrine in some states, the lesson is that care in drafting and an understanding of the law of the state in which the policy is issued are of the utmost importance in insurance policies.

House Bill Would Eliminate Learned Intermediary Doctrine In Pharmaceutical AND Non-Pharmaceutical Products Cases

Congressman Bob Filner (D-CA) has introduced the Consumer Protection Act of 2011, H.R. 542, which would “...eliminate the learned intermediary defense to tort claims based on product liability, and for other purposes.”

The legislation would repeal the Learned Intermediary Doctrine, a legal doctrine well established in many jurisdictions that provides a defense for pharmaceutical and medical device manufacturers in failure to warn claims. The Learned Intermediary Doctrine is an exception to the general rule that a product manufacturer has a duty to warn the consumer of the risks associated with the use of its product.  Under the Learned Intermediary Doctrine a manufacturer raises the defense that it had only a duty to adequately warn the “learned intermediary” (who stands between the manufacturer and consumer) of the risk associated with the use of its product.  The theory of the doctrine being that the “learned intermediary” is in the best position to understand and warn the end consumer of the product’s risks.  Over the years however, several exceptions have eroded the application of the doctrine: vaccinations, contraceptives, drugs withdrawn from the market, and direct to consumer advertising.   

When the medicine that was supposed to heal us, instead harms us, we should be able to hold drug manufacturers responsible,” “This legislation puts the power back in the hands of the consumer and makes drug companies accountable for their products.

- Congressman Bob Filner. 

While the Learned Intermediary Doctrine is generally understood to apply only in pharmaceutical related actions and to involve a manufacturer-doctor-patient relationship chain, H.R. 542 is so broadly worded that it has the potential to include any product whether a pharmaceutical or a tractor trailer.  In its apparent simplicity, the Bill could effectively shut the door on any defense that includes a "sophisticated intermediary."  Further, H.R. 542 raises significant preemption issues as it would encompass “...any tort claim in any court in the United States...”

H.R. 542  was introduced on February 8, 2011 and has no co-sponsors.  It has been referred to Committee.  H.R. 542 is in the first step in the legislative process and will first go to committee where it will deliberated, investigated, and revised it before it would go to general debate. The majority of bills and resolutions never make it out of committee.  The full text of the Bill is below.

 112th CONGRESS

1st Session

H. R. 542

To eliminate the learned intermediary defense to tort claims based on product liability, and for other purposes.

IN THE HOUSE OF REPRESENTATIVES

February 8, 2011

Mr. FILNER introduced the following bill; which was referred to the Committee on the Judiciary


A BILL

To eliminate the learned intermediary defense to tort claims based on product liability, and for other purposes.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

This Act may be cited as the ‘Consumer Protection Act of 2011’.

SEC. 2. LEARNED INTERMEDIARY DEFENSE.

(a) In General- It shall not be a defense to any tort claim in any court in the United States that a manufacture of a product has fulfilled that manufacturer’s duty of care when the manufacturer provides all of the necessary information to a learned intermediary who then interacts with the consumer of the product.

(b) Definition- In this section--

(1) the term ‘learned intermediary’ means a person, licenced under applicable State or Federal law, to advise a consumer whether or not to use the product in question; and

(2) the term ‘State’ includes the District of Columbia, Puerto Rico, and any other commonwealth, possession, or territory of the United States.