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b2ap3_thumbnail_johnson.jpgA bedroom mirror reflects a young woman, hand on her arm, facing a worn teddy bear and plastic bottle of Johnson’s baby powder. The 1980s advertisement claims “It’s a feeling you never outgrow. The powder that kept you feeling soft as a baby keeps you feeling soft today. Johnson’s baby powder. It’s the softest powder there is.” Alleged “softness” aside, recent studies have shown genital use of powder is linked with 44 percent higher risk for ovarian cancer.

 

A number of lawsuits against Johnson & Johnson have brought the cancerous risks of talc (the main ingredient in Johnson’s Baby Powder) to the public’s attention. 49 year-old Deane Berg of Sioux Falls, S.D., an everyday user of the product for over 30 years, understood the talcum powder as the probable cause of her advanced ovarian cancer almost immediately.

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Xarelto prescription side effects, Chicago product liability lawyerHave you or a loved one been prescribed Xarelto and experienced adverse side effects, such as stroke, hemorrhaging, or even death? If so, you are not alone. Reports of undesirable side effects are on the rise.

Xarelto is often prescribed to help reduce the risk of stroke or blood clots due to Atrial Fibrillation or after a hip or knee replacement surgery. It may also be prescribed to treat Deep Vein Thrombosis (DVT).

Last year, the FDA sent a warning letter to Johnson & Johnson, Inc. for false and misleading representation minimizing the risks associated with taking Xarelto in WebMD magazine advertisement. Johnson & Johnson, Inc. minimized the risk of pathological bleeding, hemorrhaging, and severe hypersensitivity to patients. The company falsely led readers to believe the side effects of using Xarelto were minimal at best.

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medical device recall, medical product liability lawyerIn an executive summary of its Medical Device Recall Report, the FDA revealed that the annual number of recalls increased by a staggering 97 percent from 2003 to 2012. Over the past decade, the complexity of medical device recalls increased and 1,190 recalls were reported in 2012, almost double the amount in 2003. Manufacturers maintain product liability for devices they market and have a responsibility to the public to alert of any potential hazards.

The FDA categorizes recalls into one of three classes. Class II recalls reflected the most significant increase in the recall report with a reported 1,043 recalls in 2012, up from 460 a decade ago.

The largest single-day recall occurred last August when Customed, a surgical kit provider out of Puerto Rico, recalled 233 of its products due to sterility issues. Other medical device recalls, such as metal-on-metal hip implants, have led to thousands of patients being affected and billions of dollars in lawsuits against its manufacturers.

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toy related injuries, Illinois product liability lawyerThe most active retail months are barely over and toy manufacturers have generated billions upon billions in revenue worldwide. The estimated cost for toy production is over two billion dollars in the United States alone as last reported in 2010. It is a booming industry that may be growing faster than safety officials can monitor.

Toys have evolved over time to include detailed parts and extra gadgets that require additional testing for their safety. They are packaged with age limit recommendations to keep babies and toddlers from choking on small pieces, but there are also unforeseen hazards in toys manufactured today which include:

  • Asbestos;
  • Carcinogens;
  • Lead; and
  • Product defectiveness.

The American Association for Justice reports a 54 percent increase of toy-related injuries from 1999-2008 ranging from choking to amputations to asphyxiation. The number of toys hitting the market largely outnumber the resources for inspection and safety tests available via the Consumer Product Safety Commission (CPSC).

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car manufacturer safety issuesThe recent air bag recalls have affected millions of Americans who own vehicles that contain the faulty equipment. Only one car manufacturer to date has taken its recall nationwide, despite the demand of the National Highway Traffic Safety Administration for others to follow suit with repairs and the hundreds of injuries that have already been reported.

The American Association for Justice (AAJ) explored how this kind of passiveness is historically common among car manufacturers. In a published report released in June 2014, the AAJ emphasizes failure on the part of these companies to take responsibility unless required to do so in court.

Among its long list of examples the AAJ names the following defective car parts corrected only after manufacturers have faced litigation:

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laproscopic surgery risk for women, FDA morcellator recallA hysterectomy ranks second behind a cesarean section ("C-section") as the most frequently performed medical procedure women undergo. In fact, the National Women’s Health Network lists statistics reporting an estimated 600,000 hysterectomies performed every year.  It is common for laparoscopic power morcellators to be used during this type of surgery as well as for myomectomies (removal of uterine fibroids). Unfortunately, nearly 1 in 350 women who undergo one of these two surgeries has unsuspected uterine cancerous tissue.

The use of laparoscopic power morcellators during either of these procedures puts women at risk of having previously undetected cancerous cells spread throughout the abdomen and pelvis. The FDA recently updated its safety alert regarding these medical devices and warns against their use during a hysterectomy or myomectomy in the majority of women. The administration emphasizes that laparoscopic power morcellators should not be used in women with suspected or known uterine cancer.

The FDA has also issued a guidance document with a manufacturer recommendation to update product labeling to include specific safety information through a boxed warning. The boxed warning advises that laparoscopic power morcellators should not be used:

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