Stryker Recall for Defective Hip Implants: Learn more from our Lawyers
According to an FDA warning letter, Stryker Corporation has manufactured defective hip replacements, resulting in injuries to patients who have received the implants. In addition to pain, patients have complained of difficulty walking, "squeaky" joints and broken implants. Some problems have meant additional surgeries for patients. According to lawyers, the very real possibility exists for a recall.
This is the second FDA warning letter Stryker Corp. has received from the FDA. Stryker claims that it is working to fix the current problems. If you have had a Stryker implant and are experiencing problems, contact us with your inquiry using the form below.
On January 22, 2008, Stryker issued a statement in response to the FDA Warning letter in which they announced the recall of Stryker hip implant devices produced in the company's County Cork, Ireland, facility.
see also:
Hip Replacement Lawsuit
Learn how to obtain a lawsuit for a problematic hip replacementFaulty hip replacement? Discover the possibility of a lawsuit.
Hip Implant Lawyer
Has your Stryker hip implant failed? Lawyers Can Help--Free Case Eval Do you know about failed Stryker hip implants? Hear from our lawyers.
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Stryker Was Warned Hip Implants Were Defective - Our lawyers are awareOur Defective Drug Lawyers are reviewing Stryker Hip Implant cases

