Faulty Hip Replacements Cause Stryker Recall

By Author: john shina
Total Articles: 7
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The Stryker hip recall started in July 2012, after a large amount of reports began coming in of tissue inflammation, bone loss, and metal ion poisoning as a result of the Stryker implants. By the time the recall had begun, tens of thousands of Stryker's defected hip replacements had already been implanted. As a result of the malfunctioning hip stems, a wave of lawsuits have erupted, as patients began having tissue inflammation and metal corrosion, which resulted in bits of rusted metal travelling down the blood stream and causing a variety of adverse effects. Many law firms have begun putting up websites specifically meant to aid people who have suffered from the malfunction.

The Stryker hip recall incident has caused the Stryker Corporation to cease production of it's Rejuvenate modular neck-hip stems. As a result of the ever increasing lawsuits, Stryker took to teaming up with Broadspire Services inc. to handle the reimbursement. As of late, the FDA has received over 60 reports of complications due to the failure of the hip implants. The high number of complaints is speculated to be the reason for the Stryker hip recall. ...
... Many people that received the failure prone hip stems were unaware of the likelihood of corrosion that the implant carried. Law firms have strongly advised that patients contact them if they have received a Stryker hip implant and are experiencing complications.

In recent news related to the Stryker hip recall, a panel of New York Judges will decide whether the Stryker lawsuits will be consolidated under a single federal judge for pre trial hearings. Many firms in the area believe that a consolidated hearing would be an efficient choice due to predicted volume of lawsuits that will come in from the failures. Currently, dozens of lawsuits are pending nationwide as enraged patients began demanding compensation for both the pain of the defected hip replacements and the cost of the surgeries to replace the corroding stems.

The necks of the implants are made of chromium and cobalt, while the stems are coated in titanium. The sliding friction between the two parts cause metallic debris to break off into the blood stream. An Urgent Field Safety Notice filed shortly before the recall, Stryker reported the implants had an increased risk for Adverse Local Tissue Reaction. Also, revision surgery has been reported as being common due to the excessive metal debris breaking off and getting into joint spaces, resulting in bone loss.

Read latest Stryker lawyer article at strykerhiprecall.net. Get all stryker hip lawsuits article with updated information.