What Damage Does Cobalt Do in My Body From a Hip?

Even though the Stryker Rejuvenate and ABGII have a much smaller metal surface area which is subject to corrosion leading to metal ions being released into the body, the harmful effects of these recalled Stryker hip implants can be just as serious.
Author: Sullo & Sullo Attorneys
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What Damage Does Chromium Do in My Body From a Hip?

Recipients of the Stryker recalled Rejuvenate or ABGII hip implants may have many questions relating to the damage one of the metals—chromium—can do to the human body. Both these Stryker models were recalled in July 2012 at which time Stryker cited the risk of fretting and corrosion, leading to the release of metal ions and a higher-than-normal failure rate.
Author: Sullo & Sullo Attorneys
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Stryker Hip Attorney Texas

The recipients of the Stryker ABGII and Rejuvenate may well need the legal representation of a Stryker Hip Attorney in Texas. These new designs by Stryker received FDA approval in 2008 and 2009, yet only a few short years later adverse reports began coming in to the FDA regarding the devices.
Author: Sullo & Sullo Attorneys
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Should I Hire a Local Attorney for My Stryker Hip?

Those who have received a Stryker ABGII or Rejuvenate hip implant are likely aware that these two implants were recalled last July, 2012. The ABGII and Rejuvenate are not “true” all-metal hip implants in that they are constructed with a ceramic ball rather than a ball made from chromium and cobalt. Nonetheless, only a few short years following FDA approval for both these Stryker models, the FDA began receiving adverse reports and Stryker sent out a field safety notice prior to the recall.
Author: Sullo & Sullo Attorneys
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Should I Hire an Attorney for My Stryker Hip?

Most victims of a dangerous drug or medical device are left reeling when they find their health has been harmed by a product they were told was perfectly safe. The Stryker Rejuvenate and ABGII hip implants were recalled in July, 2012, after only a few short years on the market. Despite gaining FDA approval in 2008 and 2009, the FDA began receiving adverse reports from consumers implanted with both devices.
Author: Sullo & Sullo Attorneys
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