What Do I Need to Do Before Having Stryker Rejuvenate or ABGII Revision Surgery?

The Continuing Effects of the Stryker Hip Recalls

August 03, 2017 - If you are one of the many people harmed by a recalled Stryker Rejuvenate or ABGII hip implant, you may have many questions about your future. More than 20,000 of the devices were sold prior to the recall in July 2012. After the recall, thousands of lawsuits were filed against Stryker for the injuries related to the devices. Some patients developed Stryker hip pseudotumors, chromium and cobalt blood poisoning...

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What Do I Need to Do to Find Out if I Have a Stryker Rejuvenate Hip Implant?

January 04, 2017 - If you heard about the Stryker hip recall which occurred in July 2012, you may have been unsure of whether your hip implant was one of the recalled devices. Both the Stryker Rejuvenate and the ABGII were recalled, due to a higher-than-normal failure rate and excessive fretting and corrosion. The Rejuvenate was...
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Pseudotumors in Stryker Rejuvenate and Stryker ABGII Metal Hip Implant Recipients

November 25, 2016 - Pseudotumors can require Stryker Metal Hip Implant Revision Surgery - Many doctors believe patients who are particularly sensitive to cobalt and chromium and other heavy metals will be more likely to develop a pseudotumor than those who are not as sensitive. A Stryker hip pseudotumor can be accompanied by tissue and bone degradation and necrosis.  When the patient...
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I Am a Stryker Hip Implant Recipient and Have Not Had a Revision—What are the Long-Term Risks of Having a Metal-on-Metal Hip?

September 27, 2016 - If you are one of the thousands of people who have a Stryker Rejuvenate or ABGII hip implant, and you have not yet undergone revision surgery, you may wonder about the long-term risks of having a recalled implant in your body. Patients with a Stryker hip device were likely dismayed to hear of the Stryker hip recall in July 2012...
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Theories of Why the Stryker Rejuvenate is Failing—Part One

June 05, 2015 - The Stryker Rejuvenate and the Stryker ABGII gained FDA approval in 2008 and 2009, but were not marketed in earnest until early 2010. Yet, little more than two and a half years later, both models were being recalled by Stryker due to a higher-than-normal failure rate as well as corrosion and fretting which could lead to excess amounts of metal debris being sheared away from the device and deposited in the hip tissues and the bloodstream...
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