Blog
Jan. 14, 2020
As a result of Hip Replacement Claims, Stryker Corporation, a major world player in the manufacture of medical equipment and orthopedic devices, on July 6, 2012, recalled two of its artificial hip implant products; the Rejuvenate Modular Hip Stem and ABG II Modular Neck Hip Stem systems. The company halted all world sales and productions of these implant devices. Victims suffered severe metal toxicity leading to painful side effects like tissue and bone death at the implant site, pain, swelling, and inflammation in the surrounding tissue, and early device failure. Stryker Hip Replacement Claims
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The Pinnacle hip replacement is a total hip replacement. The Pinnacle Hip Replacement is designed and manufactured by DePuy, the makers of the recalled DePuy ASR metal-on-metal hip. The DePuy Pinnacle hip replacement system, when used with a metal liner, becomes a metal-on-metal hip device similar to the DePuy ASR and other metal-on-metal designs. This can cause several problems in the body. The problems occur with metal shavings leaching into the body from the constant grinding of the metal joint.
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The FDA acknowledged that there are serious complications associated with vaginal mesh or bladder slings for transvaginal POP repair. There have been thousands of reports from patients, regarding serious injuries and complications occurring as a result of the vaginal mesh and bladder sling.
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If you or a loved one used either Johnson & Johnson Baby Powder or Shower to Shower Talcum Powder for feminine hygiene on your genital area and later received a diagnosis of ovarian cancer, then you may have grounds to file a lawsuit. Gerald R. Stahl will investigate your situation and advise you on your right to file a claim.
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