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From
the editors of Wolters Kluwer Law & Business, this update describes
important developments from CCH products liability and safety publications.
If you have any comments or suggestions concerning
the information provided or the format used, we'd like to hear from you.
Please send your comments to pamela.maloney@wolterskluwer.
Products Liability
U.S. Supreme Court Denies Review of
Ohio Products Retroactivity Rule
A request by the estate of a steel mill employee who was exposed to asbestos
insulation products to review the Ohio Supreme Court's decision in DiCenzo
v. A-Best Products Co., Inc., CCH Products Liability Reporter
¶18,162
(ip
access user), was denied by the U.S. Supreme Court (Dkt. No. 08-932).
The Ohio high court held that its 1977 decision [CCH Products
Liability Reporter ¶8280] that imposed strict liability
on nonmanufacturing sellers of defective products did not apply retroactively
to products sold before the state high court's earlier decision was rendered,
and applied prospectively only so that a supplier to the steel mill of
insulation products containing asbestos was not liable under a theory
of strict products liability for the death of the employee who was exposed
to the products during his employment at the mill. The question presented
asked whether the selectively prospective application of a new state common
law rule violated the Equal Protection clause of the United States Constitution.
Review of FMVSS Preemption Sought in
Light of Wyeth
In light of the U.S. Supreme Court's recent ruling in Wyeth v. Levine
[CCH Products Liability Reporter ¶18,176
(ip
access user)], the parents of a child who died as a result of injuries
sustained in a front-end motor vehicle collision have asked the High Court
to review the decision by a California appellate court in Williamson v.
Mazda Motor of America, Inc. [CCH Products Liability Reporter
¶18,206
(ip
access user)], which determined that the parents' products liability
action against the manufacturer of the minivan in which they were riding
was preempted because it conflicted with Federal Motor Vehicle Safety
Standard (FMVSS) 208 (49 C.F.R. §571.208). To the extent that the
parents’ complaint sought to hold the manufacturer liable for choosing
the lap-only seatbelt option for the rear inboard seat position, the California
court said that a successful outcome in the parents’ case would
bar automobile manufacturers from employing one of the passenger restraint
options authorized by FMVSS 208 and effectively require them to install
only lap/shoulder seatbelts to avoid liability under California law. Such
an outcome was an obstacle to the implementation of the comprehensive
safety scheme promulgated in FMVSS 208 and was, therefore, preempted,
the court concluded. The court also ruled that the parents' failure to
warn claim was preempted because it was based on their defective design
claims. In their petition for certiorari (Docket No. 08-1314), the parents
asked the Supreme Court to determine whether, in those instances in which
Congress has provided that compliance with a federal motor vehicle safety
standard does not exempt a person from common law liability, a federal
minimum safety standard allowing vehicle manufacturers to install either
lap-only or lap/shoulder seatbelts in certain seating positions impliedly
preempts a state common-law claim alleging that the manufacturer should
have installed a lap-shoulder belt in one of those seating positions.
The parents also asked whether under the High Court's ruling in Wyeth,
a federal motor vehicle safety standard allowing automakers to choose
a seat belt option impliedly preempted a state tort claim alleging that
the automaker should have warned consumers of the known dangers of a lap-only
seatbelt installed in one of its vehicles.
Questions Certified to Determine Smoker's
Injury Date
The questions of (1) when, under California law, may two separate physical
injuries arising out of the same wrongdoing be conceived of as invading
two different primary rights, and (2) whether, under California law, may
two separate physical injuries—both caused by a plaintiff's use
of tobacco—be considered "qualitatively different" for
the purposes of determining when the applicable statute of limitations
begins to run were certified to the California Supreme Court by the U.S.
Court of Appeals for the Ninth Circuit. A smoker filed a number of claims
against tobacco companies—including negligence, product liability,
and pre-1969 failure to warn—for injuries allegedly resulting from
her smoking tobacco products from 1953 until 1991. In 1989, the smoker
was diagnosed with chronic obstructive pulmonary disease (COPD), and then
in 1990, she was diagnosed with periodontal disease, both of which she
believed were caused by smoking. She did not bring suit against the tobacco
companies for these ailments. In January 2003, however, the smoker was
diagnosed with lung cancer, and under a year later she filed suit against
the tobacco companies seeking relief for the lung cancer only. The district
court held that the smoker's claims were time-barred because her "awareness
by the early 1990s that she suffered from serious smoking-related illnesses
started the statute of limitations running as to her personal injury claim."
The Ninth Circuit said that the California Supreme Court's resolution
of the certified questions will determine the outcome of the smoker's
pending appeal: if the state high court decides that, under California
law, either the smoker's 1989 diagnosis of COPD or her 1990 diagnosis
of periodontal disease started the limitations period for all tobacco-related
physical injuries, then her current suit for damages caused by her terminal
lung cancer will be time-barred and the district court's dismissal of
her complaint will be confirmed; conversely, if the California court concludes
that the limitations period did not begin with either of the smoker's
prior diagnoses, then the district court's dismissal will be reversed
and remanded for further proceedings consistent with the California Supreme
Court's decision. (Pooshs v. Phillip Morris, Inc. (9th Cir.)
CCH Products Liability Reporter ¶18,201
(ip
access user))
Purchaser of Baby Seat Lacked Standing
to Represent Class
A class action lawsuit asserting
causes of action related to products liability brought against the maker
of a baby seat was dismissed by a federal district court in California
because the purported class representative did not allege that she, or
a child on whose behalf she brought the action, sustained any injury or
property damage from use of the seat and, therefore, the court determined
that she lacked standing to maintain the action. The purchaser also failed
to allege that the seat she purchased contained any of the alleged defects.
The baby seat was designed to seat babies from as young as 3 months up
to an age of approximately 14 months independently in an upright sitting
position. In 2007, after the purchase of the seat in question, lawsuits
were filed in various jurisdictions alleging damages from severe physical
injuries to babies who had fallen out of the seats. In October 2007, the
Consumer Products Safety Commission (CPSC) issued a recall noting that
out of about one million units sold, it had received 28 reports of young
children falling out of the seat. Injuries included three skull fractures
which occurred when the seat was placed on a table. CPSC advised consumers
never to use a seat on an elevated surface or to leave a child unattended,
and to contact the manufacturer to obtain a warning label to affix to
the seat. According to the court, the purchaser's failure to allege any
injury, including the cost of a replacement product, and her failure to
show that the seat she purchased was defective negated standing and, thus,
the court did not have jurisdiction over the claim. (Whitson v. Bumbo
(N.D. Cal.) CCH Products Liability Reporter ¶18,211
(ip
access user))
Design Defect Claim Against Vaccine
Maker Preempted
The National Childhood Vaccine
Injury Act (Act) preempted design defect claims against a manufacturer
of a diphtheria-pertussis-tetanus (DPT) vaccine by the parents of a child
who developed a residual seizure disorder and encephalopathy after receiving
three doses of the DPT vaccine, the U.S. Court of Appeals for the Third
Circuit ruled. The Act contained an express preemption provision that
the vaccine manufacturer argued preempted all claims arising from allegations
of design defect. The court found that the structure and purpose of the
provision made clear that Congress intended to preempt some design defect
claims, and that the legislative history identified the scope of the preemption
to encompass both strict liability and negligent design defect claims.
In addition, the court ruled that the child's parents failed to produce
sufficient evidence upon which a jury could conclude that the vaccine
the child received came from a "hot lot"—i.e., a lot of
the vaccine associated with two or more deaths, in some cases—to
support their failure-to-warn claim against the vaccine's manufacturer.
Although the Act expressly preempted failure-to-warn claims based on "the
manufacturer's failure to provide direct warnings to the injured party
(or the injured party's legal representative)," nothing in the Act
expressly barred claims based on failure to warn "doctors and other
medical intermediaries." The parents alleged that the manufacturer
was liable for failing to warn their child's doctor that the vaccine their
child was administered came from a lot with at least two deaths and more
than thirty injuries. Under the Act, proper directions and warnings are
presumed when a manufacturer has complied with requirements under the
Federal Food, Drug, and Cosmetic Act. Once the burden shifted to the parents
to rebut the presumption, however, the court determined that they failed
to produce evidence sufficient for a reasonable jury to find in their
favor. Finally, the parents' manufacturing defect claim based on a strict
liability theory also failed due to insufficient evidence, the court held.
The parents alleged that the vaccine manufacturer's "manufacturing
process and inadequate quality control resulted in recurrent problems
with maintaining the appropriate balance between neuron-toxins and endo-toxins"
in the vaccine. Although the parents asserted that the vaccine lot used
on their injured child was tainted in that it was associated with two
deaths and more than 66 injuries, their evidence was insufficient for
a jury to conclude that their child was administered a vaccine from a
"hot lot." (Bruesewitz v. Wyeth, Inc. (3rd Cir.) CCH
Products Liability Reporter ¶18,194
(ip
access user))
No Express Preemption for State Claims
Against Trailer Maker
Products liability claims by
occupants (and their representatives) of an automobile involved in a collision
with a tractor trailer against the manufacturer of the tractor trailer
under the Connecticut Product Liability Act were not expressly preempted
by Federal Motor Vehicle Safety Standard 108, promulgated by the National
Highway Traffic and Safety Administration (NHTSA), even though the tractor
trailer manufacturer fully complied with the safety standard which governed
lighting requirements, the U.S. District Court for the District of Connecticut
held. The occupants' complaint contended that the tractor trailer was
unreasonably dangerous for its normal and intended use. The court held
that because the language of the Federal Motor Vehicle Safety Act and
Standard 108 were supportive of allowing the states to set safety standards
stricter than those Congress had set, there was no express preemption
in the case. Further, the court also found that without more evidence
concerning suggested safety modifications as part of the occupants' design
defect claims, the occupants' motion for judgment on the pleadings was
premature as to the affirmative defenses of implied preemption and conformity
with federal statutes and standards. (Bradley v. Fontaine Trailer
Co., Inc. (D. Conn.) CCH Products Liability Reporter
¶18,200
(ip
access user))
Preemption of Warning Claims for Generic Drugs Upheld
Federal law preempted state
failure-to-warn claims involving generic drugs approved under the Food
and Drug Administration's (FDA) Abbreviated New Drug Approval (ANDA) procedure,
the U.S. District Court in the Western District of Kentucky held. In two
separate cases, the patients alleged that when they took the prescription
drug, metoclopramide, to treat gastric reflux symptoms, the use of the
drug caused them to develop severe and persistent Tardive Dyskinesia,
a neurological disease. The patients' complaints against the drug's manufacturer
asserted that the manufacturer failed to adequately warn the patients
of the long-term negative effects of ingesting metoclopramide. The patients'
assertion that there was no conflict between state and federal generic
drug labeling requirements was rejected by the court, and there were no
compelling public policy reasons for the court to reconsider its prior
decisions. (Wilson v. PLIVA, Inc. (W.D. Ky.) CCH Products
Liability Reporter ¶18,195
(ip
access user); Morris v. Wyeth, Inc. (W.D. Ky.) CCH
Products Liability Reporter ¶18,196
(ip
access user))
Holster Maker Subject to Express Warranty
Claim
Proof of causation was sufficient
in an express warranty action by a former police officer against the manufacturer
of a pistol holster to raise a question of fact for the jury as to the
manufacturer's liability for the officer's injuries, a federal district
court in Mississippi held. The officer alleged that the pistol holster
which he purchased did not conform to warranties made by the manufacturer,
specifically to representations made in advertisements claiming a high
difficulty that a potential suspect would encounter if attempting to remove
a pistol from the holster. However, the officer encountered a DUI suspect
who managed to remove the pistol from the holster and fired a round in
the officer's back, paralyzing him from the waist down. The officer alleged
that during the struggle between the suspect and himself, it took the
suspect "less than five seconds" to retrieve the pistol from
the holster, a time frame the officer alleged to be unreasonably short.
Under the Mississippi Products Liability Act, the officer, as an express
warranty plaintiff, was required to prove that he "justifiably relied"
upon an express warranty in "electing to use the product." Also,
a previous Mississippi Supreme Court decision established a forgiving
causation standard for express warranty plaintiffs. Although there was
no evidence that the officer heard or read any representation from the
holster manufacturer, the officer testified that he heard of the holster's
weapon retention qualities from fellow police officers, and provided a
2002 advertisement for the holster in which the manufacturer praised the
weapon retention qualities of the holster with the language, "Hard
to Grab, Easy to Draw." Thus, the court determined, it was apparent
that the manufacturer's advertisement included specific representations
that it would be "extremely difficult" to grab a weapon from
the holster. Finally, even though the officer did not offer expert testimony,
there was a videotape of the shooting incident that would be available
for showing to the jurors. (Johnson v. Michaels of Oregon Co.
(N.D. Miss.) CCH Products Liability Reporter ¶18,207
(ip
access user))
Product Safety
President Expands CPSC; Nominates Tenenbaum
New Chair
Inez Moore Tenenbaum has been
nominated by President Obama as Chair of the Consumer Product Safety Commission
and Robert S. Adler has been nominated as a new Commissioner. President
Obama will expand the CPSC from three Commissioners, with which it has
operated for fifteen years, to five. If confirmed, Robert Adler would
fill one of these positions. In addition, the President's budget calls
for the CPSC to receive $107 million, a 71 percent increase in resources
since FY 2007. (White House Press Release, May 5, 2009)
Firms to Pay More Than $1 Million in
Outerwear Settlement
Fourteen firms have agreed to
pay $1,055,000 in civil penalties to provisionally settle allegations
that they failed to report to the CPSC, as required by federal law, that
their children's hooded sweatshirts, jackets, or sweaters were sold with
drawstrings at the hood and neck. The firms are Bob’s Stores Corp.,
The Bon-Ton Stores, Inc., Brents-Riordan Co., LLC, Concord Buying Group,
Inc., Coolibar, Inc., Forman Mills, Inc., Kidz World, Inc., Marshalls
of MA, Inc., Orioxi International Corp., Outfitter Trading Company LLC,
Retco, Inc., Seventy Two, Inc., The TJX Companies, Inc., and Urgent Gear,
Inc. The products, which pose strangulation hazards, have been recalled.
(CCH Consumer Product Safety Guide ¶57,093
(ip
access user))
Mega Brands to Pay $1.1 Million Penalty
for Violations
In a provisionally accepted
settlement agreement, Mega Brands America, Inc., f/k/a Rose Art Industries,
Inc., was fined $1,100,000 in civil penalties for failing to provide timely
information about dangers to children posed by Magnetix magnetic building
sets, as required under federal law. Mega Brands America, Inc. is a New
Jersey corporation located in Livingston, NJ. Rose Art was wholly owned
by Jeffrey Rosen, Lawrence Rosen, and Sydney Rosen until purchased by
Mega Bloks, Inc. on July 26, 2005. Mega Brands, Inc. f/k/a Mega Bloks,
Inc. is a Canadian corporation located in Montreal, Quebec, Canada. Mega
Brands is the parent company of Mega Brands America. Rose Art designed
and manufactured the Magnetix magnet toys subject to the settlement agreement
and order. (CCH Consumer Product Safety Guide ¶57,099
(ip
access user))
Information Collection Approved for
Lead-Containing Products
In conjunction with a final
rule [CCH Consumer Product Safety Guide ¶42,002] establishing procedures
and requirements for determinations that a commodity or class of materials
does not exceed specific lead limits, the CPSC submitted an information
collection which has been approved by the Office of Management and Budget.
Because the rule required manufacturers to provide certain information
along with any request for a Commission determination or exclusion, the
rule contained “collection of information requirements.” The
approval expires on March 31, 2012. (CCH Consumer Product Safety
Guide ¶57,098
(ip
access user))
Safety Standard on Roof Crush Resistance
Upgraded
As part of a comprehensive plan
for reducing the risk of rollover crashes and the risk of death and serious
injury in those crashes, the National Highway Traffic Safety Administration
has issued a final rule upgrading the agency’s safety standard on
roof crush resistance. First, the rule doubles the amount of force the
vehicle’s roof structure must withstand in the specified test, from
1.5 times the vehicle’s unloaded weight to 3.0 times the vehicle’s
unloaded weight for vehicles currently subject to the standard, passenger
cars and multipurpose vehicles, trucks and buses with a gross vehicle
weight rating (GVWR) of 2,722 kilograms (6,000 pounds) or less. Second,
the rule extends the applicability of the standard so that it will also
apply to vehicles with a GVWR greater than 2,722 kilograms (6,000 pounds),
but not greater than 4,536 kilograms (10,000 pounds). The rule establishes
a force requirement of 1.5 times the vehicle’s unloaded weight for
newly included vehicles. Third, the rule requires all of the above vehicles
to meet the specified force requirements in a two-sided test, instead
of a single-sided test, i.e., the same vehicle must meet the force requirements
when tested first on one side and then on the other side of the vehicle.
Fourth, the rule establishes a new requirement for maintenance of headroom,
i.e., survival space, during testing in addition to the existing limit
on the amount of roof crush. The rule also includes a number of special
provisions, including ones related to leadtime, to address the needs of
multi-stage manufacturers, alterers, and small volume manufacturers.
New Consumer Program for Child Safety
Seats Announced
As a result of a comprehensive
review to improve child passenger safety and federal child seat standards,
the U.S. Department of Transportation announced the creation of a new
consumer program to help parents and caregivers find a child seat that
fits in their vehicles. Secretary LaHood also ordered the National Highway
Traffic Safety Administration to develop a new side impact safety standard
for car seats. (DOT News Release, #57-09, April 24, 2009, CCH
Consumer Product Safety Guide, Report No. 938, May 11, 2009)
Motorcoach Safety Review Ordered by
DOT
A full departmental review of
motorcoach safety, ordered by U.S. Transportation Secretary Ray LaHood,
will be used to create a Motorcoach Safety Action Plan. The plan will
outline the steps needed to improve motorcoach safety. The National Highway
Traffic Safety Administration, the Federal Motor Carrier Safety Administration,
the Federal Highway Administration, and the Pipeline and Hazardous Materials
Safety Administration will participate in the creation of the action plan.
(DOT News Release, #59-09, April 30, 2009, CCH Consumer Product
Safety Guide, Report No. 938, May 11, 2009)
Request to Amend List of Child Restraints
Denied
A petition for rulemaking submitted
by the Alliance of Automobile Manufacturers requesting that NHTSA amend
the provisions of FMVSS No. 208, “Occupant crash protection,”
that apply to the selection of child restraint systems for testing advanced
air bag systems was denied. Among other things, the Alliance requested
that the agency commit to amending the list of child restraints in Appendix
A of FMVSS No. 208 every three years and allow manufacturers the option
of certifying vehicles to any edition of Appendix A for five model years
after the edition first became effective. The agency stated that the requests
were not conducive to maintaining the appendix, did not ensure child restraints
were representative of the current fleet for testing with advanced air
bag systems, and were unnecessarily restrictive. (CCH Consumer
Product Safety Guide ¶57,124
(ip
access user))
Satisfying Testing Requirements for
the CPSIA By Susan Kavanagh, CCH Washington Writer
The Consumer Product Safety
Improvement Act of 2008 (CPSIA) imposes numerous testing and certification
requirements while providing very little guidance on how to comply with
the requirements, according to Peter L. Winik of Latham & Watkins
LLP. Winik spoke about satisfying testing requirements while managing
costs in a presentation at the American Conference Institute’s National
Forum on Imported Product Safety Compliance held in Washington, DC on
April 22, 2009. (CCH Consumer Product Safety Guide, Report
No. 938, May 11, 2009)
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