Victims who have been injured from a defective product are well advised to seek the help of an experienced California products liability lawyer. The complexity of a defective product case will vary based on a number of factors.
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Toyota has announced a defective auto product recall involving about 95,700 Toyota Scions and Corolla that were sold in 19 U.S. states where cold weather could trigger a brake-related problem. According to a CBS news report, the recall affects some 2009 and 2010 Corolla and Corolla Matrix models as well as 2008 and 2009 Scion xD vehicles. If the cars are driven in extremely low ambient temperatures, there is a possibility that the condensed moisture from the positive crankcase ventilation port may seep into the brake system vacuum port and freeze, according to a company statement.
This ice build up in the brake system vacuum port can ultimately plug the vacuum port. As a result, power assist to the brakes would gradually decrease and lead to lengthened vehicle stopping distances. Owners of the recalled Toyota cars will begin to receive their safety recall notifications by mail next month. When the recall begins, Toyota dealers will install a newly designed air connector, which relocates the brake system vacuum port, for free. No other Toyota, Lexus or Scion vehicles are involved. So far, no injuries have been reported as a result of this vehicle defect.
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The California auto defects lawyers of Bisnar | Chase have filed a product liability injury lawsuit against Ford Motor Corporation, Continental Tire Corporation, TRW Vehicle Safety Systems, Chino Hills Ford, and Beceril Tire Shop.
The product liability injury lawsuit stems from injuries sustained by Griselda Bernardino during an August 2007 rollover car crash. Griselda was driving a 2003 Ford Expedition SUV when the car's left tire tread separated from the tire. This caused the Expedition to oversteer and eventually roll over. Griselda suffered severe and permanent spinal and head injuries while her passengers Ayari Martinez, Alonso Martinez, Diana and Bianca Orozco (both minors) and Maleni Elizardi (also a minor) were all seriously hurt.
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The California auto defect lawyers of Bisnar | Chase recently filed a wrongful death lawsuit against Toyota Corporation and Courtesy Toyota of Brandon, Florida. The case stems from the death of Elisa Obediente in a May 2009 rollover crash.
The car accident occurred when Elisa, a loving wife and mother of four, lost control of a 1998 Toyota 4Runner SUV that had been sold by Courtesy Toyota. According to the lawsuit, Elisa was trying to avoid another vehicle when her SUV over steered.
"We're alleging that the lateral instability of the 4Runner made it impossible to regain control of the SUV by anyone but a professional driver," said John Bisnar of the Bisnar | Chase auto defects law firm.
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The California Zicam lawyers at Bisnar | Chase continue to receive inquiries regarding lawsuits and class-action suits about defective over-the-counter Zicam cold medications, which have apparently caused hundreds of Americans to lose their sense of smell and/or taste. These Zicam defective products were meant to relieve cold congestion. However, the defective Zicam nasal cold remedy products clearly have done more harm than good.
Matrixx Initiatives Inc., the manufacturer of the Zicam cold remedies that are believed to be responsible for hundreds of users nationwide losing their sense of smell is expecting to face more Zicam lawsuits, in addition to the ones already filed, after the U.S. Food and Drug Administration warned consumers about Zicam drug effects, according to a Dow Jones news report. Last month, federal officials cautioned consumers to stop using Zicam cold and allergy medications because they can cause permanent loss of smell.
Matrixx officials have said that they are facing a lot of legal action including two economic Zicam class-action lawsuits and a personal injury lawsuit involving 117 plaintiffs. They are now saying that additional Zicam lawsuits involving individual plaintiffs making allegations that its nasal gel products have caused a permanent loss or diminishment of the sense of smell or smell and taste, have been filed. Matirxx officials have also said that they absolutely disagree with the FDA's stance that these drugs are dangerous and defective and that they intend to vigorously defend each and every one of these lawsuits. However, Matrixx has started a formal recall of all of its Zicam Cold Remedy Nasal Gel and Zicam Cold Remedy Nasal Swab products in a move to comply with the FDA's request.
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The General Motors-Chrysler bankruptcy has caused much anxiety among consumers because it seeks to throw out auto product liability and personal injury lawsuits against them. Now, a new report predicts that a loophole created by the bankruptcies of General Motors and Chrysler will make it possible for the companies to avoid issuing product recalls of defective cars that were manufactured prior to the bankruptcy filings.
According to a news article on Consumer Reports, this new report released by Safety Research and Strategies (http://www.safetyresearch.net/chrysler-gm-bankruptcy) looks into the implications of a provision in the GM and Chrysler bankruptcies that allows the automakers to avoid liability for the vehicles made before the bankruptcy. The report projects that based on information provided by both GM and Chrysler and the National Highway Traffic Safety Administration (NHTSA), more than 3,400 Americans will be injured or killed by a defective Chrysler of GM vehicle during the first year after the bankruptcy.
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Most Zicam lawsuit lawyers have seen recent warnings of the drugs effects. These effects can be devastating and the recent warnings about Zicam intranasal products, which are believed to cause a loss of sense of smell among users, is another example of that. A news article in the Associated Press talks about David Richardson of Greensboro, North Carolina, who believed he was taking a "homeopathic cold remedy" when he used Zicam's cold gel. With one squirt of Zicam cold gel, Richardson lost his sense of smell.
Here's how Richardson describes his loss to the Associated Press: "It's like watching a sunset in black and white. The things that you take for granted, not only smelling fresh-cut grass or bread in the oven…you miss those parts of your life. There's not a day that goes by that you're not reminded of it."
The U.S. Food and Drug Administration (FDA) warned consumers against three Zicam products -- Zicam Cold Remedy Nasal Gel, Nasal Swabs and discontinued Swabs in Kids' Size. Apparently, Zicam belongs to an under-the-radar, but legal sector of the drug industry called homeopathic remedies. Many drug injury attorneys have seen these pharmaceutical drugs sold over-the-counter without prescription as legal drugs claiming to treat specific aliments, yet they are not routinely reviewed for safety or benefit by the FDA. Matrixx Initiatives, the company that makes Zicam, still maintains Zicam is safe and has not yet issued a product recall. All that the company has agreed to, so far, is to suspend shipments and reimburse customers who want refunds.
Most California Zicam lawyers are aware of the recent warnings issued by the U.S. Food and Drug Administration (FDA). The FDA has warned consumers against using three Zicam cold remedy products containing zinc, after receiving more than 130 reports of serious Zicam side effects, particularly loss of the sense of smell. According to the FDA alert, many users said they lost their sense of smell with the first dose of Zicam. Others said they lost their sense of smell after repeated use of the defective Zicam products. The three Zicam products that the FDA is warning consumers against are:
The FDA is saying that consumers who have been using or are about to use these over-the-counter Zicam cold medications must stop immediately because they are associated with a condition known as anosmia or loss of sense of smell. This condition, officials say, may be either long lasting or permanent. This type of pharmaceutical drug negligence can cause serious problems to anyone that uses these recalled Zicam products.
Loss of one's sense of smell is a serious problem that can not only adversely affect a person's quality of life, but it can also be a real danger because it limits a person's ability to detect the smell of gas or smoke or other signs of danger in the environment. FDA officials have apparently issued Matrixx Initiatives, manufacturer of these defective Zicam products, a warning letter stating that these products cannot be marketed without FDA approval.
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Raptiva brain damage lawyers have continued to see new cases. Recalling the psoriasis drug Raptiva from the market due to possible risk of brain damage has left many psoriasis patients anxious and concerned about the horribleRaptiva side effects they may suffer as a result of taking Raptiva for years. According to an article in Lawyers and Settlements, some Raptiva users have been taking it for years and are just now finding out that they may be at risk for serious brain damage, even death. Genentech, the pharmaceutical company that made this drug, apparently knew about the possible side effects based on tests done overseas. But the results of those tests were never made public here in the United States.
Raptiva users could suffer PML or progressive multifocal leukoencephalopathy that reportedly leads to a deterioration of the nervous system eventually causing irreversible brain damage. Raptiva users with weakened immune systems are most at risk. Longer and continuous use of Raptiva may further increase the risk of severe side effects. The article gives the example of a patient who only took it only for six months and experienced horrible side effects. He had a severe Raptiva allergic reaction. Most patients report experienced a severe burning sensation from head to toe. This patient says that he had to be given morphine by IV because of unbearable pain and that he "looked like I was dipped in the Burger King deep fryer." Then, he lost use of his legs for close to a week. He ended up spending three months in the hospital.
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Selective Imports, a Los Angeles company that imported 80,000 tubes of toxic toothpaste from China, has pleaded no contest in court and agreed to pay $33,000 in fines to a local charity, according to this news report. The poisonous toothpaste, which was made in China, was apparently sold in the United States as Cooldent. The contaminated Cooldent toothpaste contained diethylene glycol (DEG), which is commonly used to make brake fluid and antifreeze. It is a known liver and kidney toxin. The company continued to sell the toxic toothpaste even after the U.S. Food and Drug Administration had issued a product recall warning consumers about this dangerous and toxic toothpaste product.
The biggest concern is that a majority of the 80,000 tubes of the toothpaste remains unaccounted even as the recall remains in effect. A recent investigation by Channel 10 revealed that the toothpaste was on sale and on shelves in three stores in California. Owners apparently were not aware of the recall. Selective Imports pleaded no contest to selling an adulterated drug product and will be placed on three years probation.
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