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GENERAL INFORMATION |
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Personal Injury Law News & Recall Articles |
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December
29, 2007 |
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Dave
Stewart's 72-year-old mother went to Stanford
University Medical Center for double knee-replacement
surgery in April. Four days later, she was dead.
To Stewart, an anesthesiologist, it seemed a
classic case of medical malpractice. After the
operation, his mother developed sharp abdominal
pain that she described as "10 on a scale
of 1 to 10," according to her medical records.
The hospital failed to diagnose the cause of
her pain and continued to treat her with narcotics.
Her vital signs became unstable and she was moved
to the intensive care unit, but she died of complications
from an untreated bowel obstruction. State regulators
cited the hospital in the case this fall. More...
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| December 26, 2007 |
The
Tennessean, "Washington
bureaucrats taking over American justice system" |
[Opinion
Article by Lieff Cabaser Attorney Mark Chalos]
Many
Americans believe that the FDA ensures that dangerous
medical products are not sold in the United States.
It doesn't. There have been numerous recent examples
of dangerous products being approved by the FDA,
only to be taken off the market after reports
of deaths and serious injuries. More... |
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December
18, 2007 |
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The nation's four biggest makers of microwave
popcorn have removed a flavoring chemical linked
to a lung ailment in popcorn plant workers
from nearly all their products. The companies
say all their microwave popcorn recipes should
be changed by January. But it might take several
months for the reformulated popcorn to replace
all the older varieties on store shelves. More... |
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December
13, 2007 |
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For one heart
patient, there will be no more agonizing over
whether the implanted device meant to save his
life might kill him instead. On Tuesday, two
months after Medtronic warned doctors and nearly
a quarter-million patients that a wire, or lead,
connecting their electronic defibrillators to
their hearts might break, the 48-year-old patient
had the lead and defibrillator removed and replaced.
It required a painstaking 90-minute operation
here at Morristown Memorial Hospital. More...
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December
13, 2007 |
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About 1 million
doses of two types of childhood vaccines are
being voluntarily recalled by Merck & Co.
because of possible microbial contamination,
and will result in a serious vaccine shortage,
health officials said yesterday. More...
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December 10, 2007 |
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Chrysler is recalling 575,417 Dodge trucks, vans and SUVs sold in Canada and the United States to repair a problem with the gearshift. The recall, announced Friday, affects Dodge Dakota trucks, Dodge Durango SUVs and Dodge Ram vans in the 2001 and 2002 model years as well as 2002 Dodge Ram pickup trucks. More...
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December 9, 2007 |
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Chrysler LLC said it will voluntarily recall more than 576,000 trucks, vans and sports utility vehicles because of a faulty gearshift.
'Nine incidents involving injuries have been identified in connection with this issue. No fatalities have been reported,' it said in a statement. More...
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December 6, 2007 |
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A federal jury awarded a couple $20.5 million Wednesday after finding that a number of companies failed to warn the husband that exposure to the fumes of their welding products could cause neurological injury. More... |
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December 6, 2007 |
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A plaintiffs' expert testified Wednesday that he thinks there was a defect in the van involved in a fatal 2003 accident. Ford Motor Co. is being sued by several plaintiffs who were passengers in the van when it crashed on Interstate 70 in Kansas. More...
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December 5, 2007 |
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The suit was filed on Nov. 8, 2005, and alleges that the defendant, Ford Motor Company, knowingly manufactured and sold its Expedition model SUV with a defective roof that collapses in rollover accidents. More...
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December
4, 2007 |
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Actor Dennis
Quaid and his wife, Kimberly, filed suit today
against a manufacturer of the blood thinner heparin,
saying the product's labeling and design contributed
to an overdose of the drug given to their newborn
twins last month. More...
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December
4, 2007 |
Associated
Press, "Correction on Ford
Explorer Rollover Dangers Settlement"
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In
a November 28, 2007 story about the settlement
of class-action lawsuits involving the Ford Explorer, The
Associated Press erroneously reported that
the settlements end all the outstanding rollover-related
lawsuits against the automotive company. The
settlements end the class-action lawsuits brought
by Explorer owners who said their vehicles had
lost value because of their perceived danger.
They do not end pending personal injury and wrongful
death lawsuits involving the Explorer, plaintiffs'
attorneys and Ford Motor Co. said.
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November 29, 2007 |
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A proposed settlement in a massive class-action lawsuit brought in Sacramento against the Ford Motor Co. would give 1 million Explorer owners in four states the opportunity to claim vouchers toward the purchase of a new Ford vehicle. More...
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November 29, 2007 |
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The off-road vehicle, the Yamaha Rhino, that Ashlyn Vargas was driving when she was killed Thanksgiving Day is the subject of lawsuits nationwide. More...
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November
28, 2007 |
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Ford Motor
Co has agreed to settle class-action litigation
covering plaintiffs in four states who claimed
its Explorer sport utility vehicles were prone
to rollovers, Ford said on Wednesday. "From
Ford's position, we believe the settlement is
fair and reasonable and in the best in interests
of our customers and our shareholders," Ford
spokeswoman Kristen Kinley said. More...
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November 23, 2007 |
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The Thanksgiving holiday takes a tragic turn when a 12 year old girl dies in an ATV accident.It happened near Highway 58 in the California Valley, just before noon Thursday. More...
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November 20, 2007 |
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When ATV
racer Brandon Leach got sideways in the air during
a race in Mammoth in April, he pretty much figured
the outcome would be bad. It was. The wheels
of the 450cc Honda TRX quad hit the ground, slamming
him into the dirt. The 350-pound vehicle then
flipped into the air and landed on him. "Right there I went
blank," Brandon, 16, said recently between
runs at Pima Motorsports Park. Brandon was airlifted
to Tucson's University Medical Center, where
a dislocated collarbone, bruised pelvis, three
cracked ribs, collapsed lung and a concussion
kept him hospitalized for 12 days. More...
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November 19, 2007 |
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Lieff Cabraser Heimann & Bernstein LLP has announced that ten contact lens solution users from across America have filed a personal injury lawsuit against Advanced Medical Optics in state court in Los Angeles, CA. More...
Learn more about AMO injuries and the lawsuit
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November 11, 2007 |
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Although few people might be willing to throw out their Chinese-made toys, a growing scandal is prompting some consumers to boycott Chinese-made products - just in time for Christmas. The latest horror story is so bizarre, it’s almost unbelievable. At least two children in the United States and four in Australia were hospitalized when they ingested beads from a popular new toy. Glue in the product contained a chemical that metabolized into what is known as the “date rape drug.” More...
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November 10, 2007 |
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About 4.2 million Chinese-made toys have been voluntarily recalled in the U.S., which could be far more dangerous than anything having to do with lead. It's an arts and crafts toy called "Aqua Dots". Tests show a coating on the toys could send your child into a coma, or worse if swallowed. More...
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November 9, 2007 |
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Seven more U.S. children
were sickened after ingesting Chinese-made toy
beads that were recalled earlier this week because
of a toxic chemical coating, the government said
Friday. The reports of the sickened children, six
of whom were hospitalized, came from at least five
states: Texas, Delaware, New Hampshire, Illinois
and Utah, according to a spokeswoman for the Consumer
Product Safety Commission. More...
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November 9, 2007 |
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Merck & Co.
said Friday it will pay $4.85 billion to end
thousands of state and federal lawsuits over
its painkiller Vioxx in one of the largest drug
settlements ever. Company officials estimated
the deal, if accepted, would end 45,000 to 50,000
personal injury lawsuits involving U.S. Vioxx
users who suffered a heart attack or ischemic
stroke, the type in which blood flow to the brain
is blocked. More...
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November 9, 2007 |
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Three years after withdrawing its pain medication Vioxx from the market, Merck announced today that it will pay $4.85 billion to settle 27,000 lawsuits by people who contend they or their family members suffered injury or died after taking the drug. More...
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November 9, 2007 |
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A popular children’s toy called Aqua Dots, also know as Aqua Beads, are being recalled after tests found chemicals in the toy that can turn into a date rape drug if swallowed. More...
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November 8, 2007 |
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Aquadots Recall - After two children swallowed Aqua Dots and became comatose, the U.S. consumer-safety regulators have recalled 4 million of the China-made arts-and-craft toys. More...
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November 8, 2007 |
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The wildly popular craft beads known in the U.S. as Aquadots have been huge sellers. Young Heather Lehane in Australia loved them, until she put them in her mouth. More...
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November 8, 2007 |
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Millions of
Chinese-made toys have been pulled from shelves
in North America and Australia after scientists
found they contain a chemical that converts into
a powerful "date
rape" drug when ingested. Two children in
the U.S. and three in Australia were hospitalized
after swallowing the beads. The recall is yet
another blow to the toy industry -- already bruised
by a slew of recalls during the summer. More...
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November
8, 2007 |
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A woman whose toddler
son ingested a popular toy that contains a chemical
that turns into a powerful "date rape" drug
when eaten said Thursday she knew he was ill
when he began to stumble, seemed drunk and started
vomiting. The mother, Shelby Esses, said her
20-month-old son Jacob, fell down and was limp
after getting into his older sister's Aqua Dots,
a Chinese-made toy recalled Wednesday by the
Consumer Product Safety Commission. More...
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November 7, 2007 |
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More toys made in China have been recalled today. Scientists have discovered that a chemical in them is the equivalent of the date rape drug GHB (gamma hydroxy butyrate,) which can cause seizures, drowsiness, unconsciousness, coma, or death.Two kids in the U.S. and three in Australia were hospitalized after swallowing beads in Bindeez and Aqua Dots. Used for arts and craft projects and sold in retail stores and over the Internet, the beads fuse together when sprayed with water. More...
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October 23, 2007 |
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When Irma Ortiz walked into Dr. Phil Harber's Los Angeles office last year, it was the end of a frustrating medical journey. For years, doctors said she had asthma. Or bronchitis. They prescribed medicine, then sent her on her way. She kept coughing. She got weaker. By December 2005, the 45-year-old woman who could once lift 50-pound boxes without breaking a sweat could work no more. More...
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October
16, 2007 |
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Hundreds
of injuries linked to a brand of heart defibrillator
wires were reported to the government by last
winter, a consumer advocate said Tuesday in asking
why the wires weren't recalled until this week.
Medtronic Inc. pulled its Sprint Fidelis defibrillation
wires off the market Monday, after identifying
five patient deaths in which broken wires may
have played a role. More...
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October
16, 2007 |
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A man
who claims he received 47 unneeded jolts from
his implanted defibrillator is suing Medtronic
over the broken wires the company is recalling.
Plaintiffs Leonard Stavish and Kelly Luisi
seek class-action status in U.S. District Court
in Minneapolis as representatives of people
they say were hurt. The lawsuit's allegations
include emotional distress and negligence,
and it seeks restitution, disgorgement of profits,
and punitive damages. More... |
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October 16, 2007 |
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More than 90,000 Americans get potentially deadly infections each year from a drug-resistant staph "superbug," the government reported Tuesday in its first overall estimate of invasive disease caused by the germ. More...
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October
15, 2007 |
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Recalls
had already battered the heart device industry
when Medtronic warned doctors that the wires
connecting a patient's heart to its implantable
defibrillators break too often. Medtronic told
doctors to stop using the Sprint Fidelis wires
after linking five deaths to breaks in them.
The company said the Fidelis wires failed slightly
more often than the thicker wires they were
meant to replace. More...
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October 11, 2007 |
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Johnson & Johnson,
Wyeth and other makers of infants' nonprescription
cough and cold products are recalling certain
medicines in the United States because of the
danger of overdose, the Consumer Healthcare Products
Association said on Thursday. Novartis and Prestige
Brands Holdings are recalling their oral infant
cough and cold medicines, as well, because data
show that when the medicines are misused, it
can lead to overdose, especially in children
under 2 years old. More...
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LLP is an over fifty attorney
law firm with offices in San Francisco, New York and Nashville. For the last five years,
the National Law Journal has recognized Lieff Cabraser
as one of the top 20 plaintiffs law firms in America. |
| For our personal injury cases, we bring a team of experienced
lawyers. Each client is assigned an individual lawyer. In addition, we have
on staff multiple nurses, legal assistants, scientific analysts and case
clerks to assist the attorneys. To learn more about our firm, click
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About Lieff Cabraser: We have
offices in San Francisco, New York and Nashville. Our lawyers have
represented clients in personal injury, wrongful death and
rollover crashes and product defect lawsuits across America, including
residents of Alaska, Alabama, Arkansas, Arizona, California,
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Among the cases our personal injury
attorneys are prosecuting are the Medtronic heart lead recall, the
AMO contact lens solution recall, the Peter Pan peanut butter recall, Guidant
pacemaker defects, SUV
rollover accidents, popcorn
workers lung injuries, and Ford
switch fires.
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