March 28, 2017 - Thousands of consumers were affected by the Stryker recall in July 2012. The recall covered both the Rejuvenate and the ABGII.  At the time of the Stryker hip recall, Stryker admitted the devices had a higher than normal failure rate, and were prone to fretting and corrosion. If you are an individual affected by the Stryker recall, you could have received a Broadspire letter...

March 16, 2017 - When Stryker first introduced the Stryker Rejuvenate in early 2010, the company claimed the device would last much longer than other metal hip implants...Soon after patients were implanted with the Stryker Rejuvenate and ABGII, adverse event reports began coming in to the FDA. Patients complained of symptoms of Stryker hip metallosis, Stryker hip blood poisoning, Stryker hip pseudotumors and Stryker hip infection...