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transvaginal mesh, Illinois product liability lawyerWomen who suffer from stress urinary incontinence (SUI) or pelvic organ prolapse (POP) may be implanted with transvaginal mesh (TVM), a medical device that gives added support when weakened or damaged tissue is being repaired. According to statistics, up to 70,000 women have this medical device implanted each year, illustrating a reliance on TVM to correct certain medical problems.

However, the American Association for Justice reported the impact of dangerous medical devices such as these in 2013 and noted that there were early detections of problems linked to TVM even during its rising popularity in the early 2000s. TVM has been known to cause:

  • Bleeding;
  • Infection;
  • Pain;
  • Erosion or hardening of the device; and
  • Difficulty in removal of the device.

Additional surgeries are required to repair complications with mesh erosion and still do not solidify a guaranteed resolution to the adverse effects originally caused by TVM. These procedures mean costly hospital stays, prolonged medical care, and a diminished quality of life for a medical device that the FDA said did not necessarily improve post-surgical outcomes in many cases.

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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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infant medical device recall, Chicago product liability attorneyPhilips Healthcare initially recalled its Gel-E Donut and Squishon 2 medical devices in May 2014 after visible mold was detected on the outer surface of the products. This recall was for devices distributed from July 2012 to December 2013.

As of October 2014, the Food and Drug Administration (FDA) reported a Class I recall issued by the same manufacturing company for the same devices. These gel-filled products are used under supervision in hospitals to support an infant’s head and body. The following models have been recalled:

  • Gel-E Donut 92025-A;
  • Gel-E Donut 92025-B;
  • Gel-E Donut 92025-C; and
  • Squishon 2 91033-2.

The second recall included products manufactured from July 2012 through to August 2014. The defective devices prompted 12 new complaints of visible mold within just four months of the initial recall. Cladosporium and Penicillium Fungi were two of the molds identified, which can cause:

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Chicago airbag recall lawyerHonda has become the first and only automotive company thus far to meet the demand from the National Highway Traffic Safety Administration (NHTSA) to repair vehicles nationwide after the recent recall of Takata airbags.

Previously, the recall for airbags were limited to high-humidity states only. An increase in humidity was found to cause the airbags to inflate too fast, leading to an explosion, which caused shrapnel to spew out.

According to a report, Honda is expanding its repairs to over 2.6 million for a total of 5.4 million vehicles. The following models are included in this expansion:

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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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