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AAJ News Brief for Haytham Faraj | Monday, March 15, 2010 |
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Leading the News
First contested bellwether case in Chinese drywall litigation to be heard this week.
The New
Orleans Times-Picayune (3/14, Mowbray) reported on Tatum and Charlene
Hernandez of Mandeville, LA, whose Chinese drywall suit will be heard this week
in the first contested "test case in the Chinese-Manufactured Drywall Products
Liability Litigation" before Judge Eldon Fallon in New Orleans. "While the
Hernandez case doesn't have any direct legal influence on the other cases, what
the court decides about what needs to be done to fix the Hernandez home and how
much it will cost to make those repairs could help establish values that will
guide settlement discussions in the rest of the cases." What Judge Fallon
"decides is potentially influential outside of the court proceedings, too," as
his "determinations...could end up becoming the de facto standard" for
remediation
efforts.
McClatchy
(3/14, Marsteller) reported, "The trial's primary goal 'is to get a remediation
protocol to guide future litigants,' said Scott Weinstein, a Fort Myers attorney
who is on the plaintiff's steering committee in the consolidated proceeding, but
is not directly involved in the Hernandez case." While "public attention will
be focused on U.S. District Judge Eldon Fallon's final decision in Hernandez,
it's the pre-trial legal maneuvering -- especially over expert witnesses -- that
could have a greater impact on later cases," said John Rainn, an adjunct
professor of construction law at Stetson University College of Law. "Attorneys
on both sides in the Hernandez suit already are challenging the other side's
experts, court records
show."
Fallon profiled.
The Palm
Beach (FL) Post (3/14, Ross) reported, "In the complex, ongoing mess
created by defective, sulfur gas-emitting drywall, U.S. District Judge Eldon E.
Fallon is regarded by many homeowners as the best hope for providing solutions."
The judge "with the soft Southern drawl and penchant for courtroom civility and
deadlines is the man whose rulings could set standards on fixing affected homes
and determining the extent of damage the wallboard has
caused."
Florida Sen. Bennett introduces bill which might limit ability to sue over
Chinese
drywall.
The Bradenton
(FL) Herald (3/13, Kennedy) reported that Florida state Sen. Mike
Bennett "has filed a bill that could limit a homeowner's or condo association's
ability to sue over defective drywall, according to attorneys representing those
dealing with contaminated property." Senate Bill 2196 "would prohibit, under
certain circumstances, legal action in connection with damage to property
arising from use of 'reactive drywall,' or from repairs necessitated by it,
according to its text." Bennett says that "the bill is still in draft form and
that he does not plan to advance it the way it is worded
now."
Florida builder claiming inability to pay for remediation recently went on
land-buying spree, records
show.
The Sarasota
(FL) Herald Tribune (3/15, Kessler) reported, "Bradenton-based
Medallion Homes has been at odds with the owners of at least a half-dozen houses
it built using contaminated Chinese drywall." Several "weeks ago, the builder's
attorney, Alan Tannenbaum, commented for the first time -- saying the reason
Medallion is not repairing the affected homes is simply that it does not have
the money to do so." But "state and county records reviewed by the
Herald-Tribune" show that "Medallion and its associated entities have recently
engaged in some of the largest land acquisitions in the Sarasota-Bradenton area,
spending millions of dollars to buy up everything from lots to entire
subdivisions."
Louisiana home builders say state should create application process for Chinese
drywall
relief.
The Baton Rouge
Advocate (3/14, Griggs) reported, "No one is sure what if any process
state or federal regulators will approve to fix problems many homeowners are
having with Chinese drywall, when a fix might happen or who would pay for it.
But the Louisiana Home Builders Association" says that "the state should
establish an application process" so that "when a remediation method is approved
and if money is made available, homeowners won't face additional delays before
getting help." In the meantime, "everyone is waiting on the scientists under
the Interagency Task Force on Chinese Drywall to figure out what exactly in the
drywall is causing all the
problems."
From the American Association for
Justice |
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Civil Justice System
Personal injury recoveries climb in 2009's "Top 100 Verdicts" list.
The National
Law Journal (3/15, Qualters) reports, "Judging by the recoveries that
National Law Journal affiliate VerdictSearch counted among its Top 100 Verdicts
of 2009," commercial verdicts fell last year. "A bright spot for plaintiffs
attorneys was personal injury causes of action. Medical malpractice awards
jumped from $321 million to $509.2 million; motor vehicle verdicts hit $738.9
million (up from $470 million); and products liability jumped to $1.1 billion
from $458 million the year
before."
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Classmates.com settles marketing class-action for $9.5M.
In the "TechFlash" blog at the Puget
Sound (WA) Business Journal (3/13), Todd Bishop wrote, "Seattle-based
Classmates.com has agreed to pay up to $9.5 million to its users to settle a
lawsuit that accused the social network of sending emails that made people
believe their old friends from high school were reaching out to connect -- only
to discover, after paying for a membership, that their long-lost buddies were
nowhere to be found. The proposed settlement, filed yesterday in U.S. District
Court in Seattle, would designate $3 in cash for every Classmates.com member
(dating back to Jan. 1, 2007) who upgraded to a 'gold' membership on the site
after receiving an email suggesting that they pay for premium access to see who
had signed their online guestbooks. Documents filed in the case estimate that as
many as 3.16 million people in the United States would be eligible for the
payout."
New Jersey SC Civil Practice Committee releases proposed rule changes.
The New
Jersey Law Journal (3/12, Gottlieb) reported, "The state Supreme Court
Civil Practice Committee has published its 2010 report of proposed rule changes:
a 169-page compendium of suggestions for fixing inefficiencies and injustices
identified by practitioners or judges. It also summarizes ideas shot down or
tabled, explaining why a proposed cure might have no impact or might be worse
than the alleged
disease."
Ways to defeat Daubert challenges discussed.
In an op-ed in the Legal
Intelligencer (3/12), Jim Ronca of Anapol Schwartz Weiss Cohan Feldman
& Smalley discusses how lawyers can prepare their cases "in a fashion that
deflates or defeats [a] Daubert challenge before it is even filed." Ronca
comments, "Before even getting involved in the case, research the medicine
extensively and consult with a good epidemiologist (one who does not simply say
what you want to hear)." He adds, "Have the expert do a comprehensive
systematic literature search for relevant
studies."
Congress
House Democrats look for final votes to pass Senate healthcare reform bill.
As momentum builds toward a healthcare reform vote in the House, many news
agencies are analyzing whether Democrats will have enough votes to pass the
legislation. The AP
(3/15, Quaid) reports that Rep. James Clyburn (D-SC), "the House's chief
Democratic headcounter, said Sunday he hadn't rounded up enough votes to pass
President Barack Obama's healthcare overhaul heading into a make-or-break week,
even as [David Axelrod,] the White House's top political adviser said he was
'absolutely confident' in its prospects." Meanwhile, the Obama Administration
"gave signs of retreating on its demands that senators jettison special
home-state deals sought by individual lawmakers that have angered the
public."
Drug Safety
US court rules thimerosal does not cause autism.
The New York
Times (3/13, A11, McNeil) reported, "In a further blow to the
antivaccine movement, three judges ruled Friday in three separate cases that
thimerosal, a preservative containing mercury, does not cause autism." The
rulings "are the second step in the Omnibus Autism Proceeding begun in 2002 in
the United States Court of Federal Claims," which "combines the cases of 5,000
families with autistic children seeking compensation from the federal vaccine
injury fund." The fund pays "families of children hurt by vaccines," but it
"has never accepted that vaccines cause
autism."
The Los
Angeles Times (3/13, Maugh, Zajac) reported, "The cases that three
judges, called special masters, chose to rule on as test cases were considered
among the strongest, so the outlook appears grim for others making the same
claim." In one case, Special Master Denise K. Vowell wrote that "petitioners
propose effects from mercury in [vaccines] that do not resemble mercury's known
effects in the brain, either behaviorally or at the cellular
level."
"The cases had been divided into three theories about a vaccine-autism
relationship for the court to consider," the AP
(3/13, Schmid) reported. The court previously "rejected a theory that
thimerasol can cause autism when combined with the measles-mumps-rubella
vaccine," and "a theory that certain vaccines alone cause autism." But,
Friday's "ruling doesn't necessarily mean an end to the dispute...with appeals
to other courts
available."
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FDA adds boxed warning to Plavix.
The AP
(3/13, Perrone) reported that the FDA "is adding its strongest warning to the
label for Plavix [clopidogrel bisulfate], cautioning that some patients do not
respond to the blockbuster blood thinner." According to the Los
Angeles Times (3/12, Maugh) "Booster Shots blog," the "warning
indicates that the drug is dangerous only in the sense that it doesn't work in"
certain "patients and thus may leave them unprotected against heart attacks and
strokes."
Specifically, some patients have a difference in a liver enzyme known as
CYP2C19, which helps to convert Plavix to a form that the body can use, Dow
Jones Newswire (3/12, Dooren) reported. Notably, FDA officials said
CYP2C19 tests typically cost less than
$500.
Robert Temple, deputy director for clinical science at the FDA's Center for Drug
Evaluation and Research, said, "What there hasn't been is a clear test of
whether you can take people who are poor metabolizers, double their dose and do
just as well," according to Bloomberg
News (3/12, Peterson,
Larkin).
Employment/Workplace Safety
Legislators seek to strengthen whistle-blower protections.
USA
Today (3/15, Eisler) reports, "Members of Congress want to give
federal whistle-blowers better safeguards against retaliation," including rights
to jury trials on retaliation claims, lifting "gag rules imposed by some
national security agencies" and strengthening rules "against penalizing
whistle-blowers who report wrongdoing to Congress." Currently the retaliation
review processes "almost always end with the same result: The whistle-blowers
lose."
Medical Errors/Healthcare
FDA investigating device maker's failure to report patient death.
The Houston
Chronicle (3/13, Ackerman) reported, "Federal regulators are
investigating whether the Houston maker of a pediatric heart pump designed by
famed surgeon Michael DeBakey should have reported the death of a patient who
got the device." In a warning letter to MicroMed Cardiovascular, the FDA
notified the company in December "that information collected during an
inspection last summer suggested that a death related to the DeBakey VAD Child
Device occurred and was not reported." An agency spokesman said that "the FDA
isn't saying the device caused the death, but because it was used on the patient
and may have caused or contributed to the patient's death, the company should
have reported the
incident."
Drug companies increasingly turning to private physicians to promote products.
The Milwaukee
Journal Sentinel (3/14, Fauber) reported, "For years, drug companies
sought out influential university doctors with impressive credentials to bring
their message to other doctors and persuade them to write prescriptions for
their products." But as "the practice of doing promotional speaking for drug
companies has come under fire in recent years," more "medical schools...have
developed conflict-of-interest policies that ban such talks." Companies have,
therefore, "been forced to back away from that approach," turning to private
physicians instead, who are not regulated by conflict-of-interest policies. As
a result, US Sen. Herb Kohl (D-WI) "has co-introduced legislation requiring
companies to release payments to doctors to highlight conflicts of interest for
the
public."
Defense attorney criticizes team's approach to hospital wage-fixing case.
The Chicago
Tribune (3/13, Sachdev) reported, "Several Chicago-area hospital
systems last month quietly settled a federal lawsuit that alleged they had
conspired to fix or depress wages that they pay registered nurses. In the
settlement, two nurses who were plaintiffs received $25,000 each, a small amount
considering the case sought to represent a class of about 19,000 nurses that
could have exposed the hospitals to nearly $1 billion in damages, according to
people involved in the matter." But John Cusack, "the veteran Chicago antitrust
lawyer who briefly worked on the case with the defense team says the hospitals
spent millions of dollars to defend what he says was a frivolous lawsuit."
Cusack has criticized the defense team's approach to the
case.
New reports suggest many Americans are being overtreated.
The AP
(3/13, Tanner) reported, "A spate of recent reports suggests that many
Americans are being overtreated." Research appearing in the New England Journal
of Medicine "suggested that too many patients are getting angiograms...who don't
really need them; and specialists convened by the National Institutes of Health
said doctors are too often demanding repeat cesarean deliveries for pregnant
women after a first C-section." Meanwhile, "the American Cancer Society cast
more doubt on routine PSA tests for prostate cancer" as "experts dispute how
much routine cancer screening saves lives." Still, "Not all doctors and
advocacy groups agree with the criticism of screening. Many argue that it can
improve survival chances and that saving even a few lives is worth the cost of
routinely testing tens of thousands of
people."
Columnist claims trial lawyer donations led to absence of tort reform in healthcare bill.
In a column in the Washington
Times (3/14), Donald Lambro criticized President Obama's "attack on the
Supreme Court's ruling that ended the ban against corporate spending for
political campaigns." Lambro comments that Obama knows "a thing or two about
opening the floodgates of campaign money," adding, "like wealthy trial lawyers
who win huge sums of money from medical liability lawsuits. The checks they
collected for his campaign were worth every million they gave him," as "his
health care reform plan dutifully left out any mention of tort
reform."
Product Safety
Driver's claims scrutinized as investigators fail to duplicate Prius acceleration.
In San Diego, the AP
(3/15, Spagat, Thomas) reports scrutiny of a Toyota Prius continued yesterday
as the driver's attorney dismissed a House Oversight and Government Reform
Committee "memo that questions his client's version of events." That memo
obtained by the AP said National Highway Traffic Safety Administration
technicians as well as Toyota "could not duplicate the sudden, unintended
acceleration that James Sikes said he experienced March 8 when he reached 94 mph
on a California
freeway."
The Los
Angeles Times (3/15, Chang) also reports the memo indicates that when
investigators who tested the car last week "pressed hard on the brake pedal and
the accelerator at the same time, the Prius' gasoline engine shut down." Sikes
had reported the car kept going, even though he was "laying on the brakes." His
attorney, John Gomez, yesterday said, "There's a ghost in the machine. And no
one is able to replicate it or pinpoint it or identify
it."
The Washington
Post (3/15, Ahrens) notes that Toyota "has said it has had difficulty
duplicating other reported incidents of runaway vehicles." Yet Kurt Bardella, a
spokesman for the committee's top Republican, Darrell Issa, yesterday said the
"findings 'certainly raise new questions surrounding the veracity of the
sequence of events' reported by Sikes." Bardella added, "We're not saying Mr.
Sikes is wrong or that he lied, we're saying that questions have arisen in the
investigation."
Fatal crashes said to show acceleration problems extend across product line.
Focusing on traffic deaths linked to Toyota vehicles, USA
Today (3/15, Carty) notes anonymous complaints in a database run by the
NHTSA and writes that it "examined 25 of the 43 fatal accidents with 52 deaths.
They are among 2,600 complaints to NHTSA since 2000 that allege sudden
unintended acceleration in Toyota products." USA Today lists trends it says
emerged in its examination of the fatal accidents, including that "allegations
of acceleration extend across Toyota's product
line."
Ohio woman says accelerator on her Lexus stuck.
The AP
(3/15) reports, "An Ohio woman says her Lexus careered through a parking lot
and crashed into a light pole in Fort Wayne, Indiana, after its accelerator
dropped to the floor. Myrna Cook was treated for a broken leg and other
injuries Thursday. ... Three spokesmen for Toyota Motor Corp., Lexus's maker,
and a National Highway Traffic Safety Administration spokeswoman did not return
calls."
Orange County, CA, sues Toyota over acceleration defects.
In a separate article, the AP
(3/12) reported, "The Orange County district attorney has filed a lawsuit
against Toyota Motor Corp., accusing the automaker of knowingly selling hundreds
of thousands of vehicles with acceleration defects. District Attorney Tony
Rackauckas said at a news conference Friday that his office has the right to
bring consumer protective action on behalf of Orange County residents." Orange
County's lawsuit "accuses Toyota of using deceptive business practices to become
the world's top
automaker."
Lawyers vying for key roles in Toyota lawsuits.
According to the Wall
Street Journal (3/15, B1, Searcey), US lawyers are vying for key roles
and influence in litigation against Toyota, which faces accusations of fraud and
of using substandard electronics connected to drivers' sudden-acceleration
claims.
Critics blast sale of "formaldehyde-tainted" Katrina trailers.
The Washington
Post (3/13, Hsu), reporting on FEMA's recent sale "for pennies on the
dollar most of the 120,000 formaldehyde-tainted trailers it bought nearly five
years ago for Hurricane Katrina victims," said the "sale of the units, perhaps
the most visible symbol of the government's bungled response to the hurricane,
has triggered a new round of charges that it is endangering future buyers for
years to come." According to the Post, "consumer advocates and
environmentalists are outraged that the government resold products it deemed
unsafe to live in, saying warning stickers attached to the units will not keep
people from misusing them." The Post noted that the "mass sale came four weeks
after a federal judge lifted a ban on the sale of some trailers, which are part
of [formaldehyde-related] litigation brought by 40,000 former Katrina occupants
against FEMA and the manufacturers." National Association of State Agencies for
Surplus Property executive director Scott Pepperman is quoted saying that FEMA
is "shoveling the whole thing under the carpet to make it go
away."
FDA investigating spice safety.
In a front-page story, the Washington
Post (3/14, A1, Layton) reported that the FDA "is reexamining the
safety of...spices." Last week federal regulators met "with the spice industry
to figure out ways to make the supply safer." FDA associate commissioner for
food safety Jeff Farrar said that the agency "wants the spice industry to do
more to prevent contamination. That would include using one of three methods to
rid spices of bacteria: irradiation, steam heating or fumigation with ethylene
oxide, a pesticide." Legislation pending in the Senate would "require food
companies to take steps, such as treating raw spices, to avoid
contamination."
Time
(3/15, Park) reports that the FDA "does not have specific guidelines for
screening lead in dried products" because it "feels there is no safe level of
lead in dried products, since studies have not yet established that lead
exposure doesn't lead to adverse health effects." The agency, however, has
"been reviewing its protocols for spices, to determine whether the risk of
contamination or exposure to elements such as lead from dried products imported
from overseas warrants more
scrutiny."
FDA considers ending third-party review process.
The Wall
Street Journal (3/15, Mundy, Favole) reports that the FDA is
considering whether to end the practice of approving medical devices based on
third-party reviews. More than one-third of the products using third-party
reviews are imaging and other radiological devices. Devicemakers use the
process to get the imaging devices to market quicker, according to the Journal.
But Donna-Bea Tillman, the head of the FDA's device-evaluation office, tells the
Journal that third-party reviewers commonly have less information on the devices
compared to the
agency.
Camel cigarette campaign appealed to teen girls.
USA
Today (3/15, Szabo) reports, "The ads for Camel No. 9 cigarettes --
which ran in magazines such as Vogue, Cosmopolitan and Glamour -- were a hit
with girls ages 12 to 16," according to a Pediatrics study. Investigators also
discovered that "promotional giveaways for the new brand...included
berry-flavored lip balm, cellphone jewelry, purses and wristbands." A
spokesperson for R.J. Reynolds "says the ads were aimed at adults, noting that
85% of the magazines' readers are over 18." But the study's co-author pointed
out that "within a year of the ads' debut, 22% of girls listed Camel as their
favorite cigarette ad," which is "twice the number" of those who previously said
so.
Illinois measure aims to reduce use of cancer-linked dry-cleaning chemical.
The Chicago
Tribune (3/14, Hawthorne) reported, "Similar to rules already adopted
in California and being considered by other states," Illinois "seeks to
dramatically reduce the use of a toxic chemical that has poisoned hundreds of
sites across the state." Under the measure supported by Gov. Pat Quinn's
administration, businesses will no longer be able to install machines that use
"perchloroethylene, or perc, a common dry-cleaning chemical linked to cancer,
liver damage and neurological problems," and they would have to stop "using the
chemical in residential buildings by 2013. All perc use would be outlawed in
2026," but owners could apply for "grants of up to $10,000 to buy new, perc-free
equipment."
Securities
Lehman bankruptcy report may guide lawsuits.
Bloomberg
News (3/13, Hurtado, Sandler) reported, "A 2,200-page bankruptcy report
a year in the making may point the way for plaintiffs looking to sue former
Lehman Brothers Holdings Inc. officials, lawyers said, rather than grand juries
probing possible crimes. The report, filed by bankruptcy examiner Anton Valukas
in Manhattan federal court on March 11, describes off-balance-sheet transactions
Lehman used to hide debt in late 2007 and 2008, deceiving shareholders about its
ability to withstand
losses."
Also in the News
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