Learn about the Stryker Inspection and Possible Recall from our Attorneys
According to an FDA warning letter, dated November 28, 2007, problems were found during an inspection of the New Jersey Stryker Facility that are directly linked to defective implant components. The inspection of the facility took place on June 12th and July 1st of last year. This is the second FDA warning to Stryker since the inspection last summer. The most recent letter faults Stryker for an inadequate responses to the first warning. According to attorneys, there is the potential for the problems to lead to a recall.
If you have a Stryker implant and are experiencing problems, please contact us your with questions or concerns in the form below.
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Inspection Information
Learn about the possible Stryker recall from our attorneysLearn from our attorneys about a possible Stryker recall
Hip Replacement Complications
Learn problems associated with hip replacements here.Do you know about the problems that come with a hip replacement?
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Stryker Was Warned Hip Implants Were Defective - Our lawyers are awareOur Defective Drug Lawyers are reviewing Stryker Hip Implant cases


