Stryker Hip Recall
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Stryker Hip Recall Lawsuits

Stryker Hip Recall Lawsuit Information

Stryker Hip Recall LawsuitStryker Corporation received FDA approval for the Rejuvenate and ABG II modular neck stem hip replacement systems through the controversial 510(k) process, which bypasses pre-market testing requirements to fast track approval. Therefore, it has taken the suffering of individual hip replacement patients to notice a trend indicating higher than expected failure rates, resulting in the Stryker hip recall.

The hip replacement components that are included in this Stryker hip recall were marketed as being safer and more reliable than other similar products such as those recalled by Stryker Orthopaedics. In fact, the Stryker hip recall was prompted by the same types of complaints and concerns. The Stryker hip recall and the one from Stryker occurred because the products have been found to cause fretting and corrosion at the modular neck stem site. When metal debris is deposited into the hip joint, patients face a range of medical problems, including pain, inflammation, instability, and potentially even problems related to the toxic metals entering their bloodstream. Stryker hip recall lawsuits are being filed on behalf of people who have suffered from a failed Stryker hip replacement system, including those who have been forced to undergo a revision surgery as a result.

Current Stryker Hip Recall Lawsuits

Lawsuits filed as a result of the Stryker hip recall will occur for a variety of reasons, depending upon what you are experiencing. All Stryker hip recall lawsuits will include all medical costs, whether they are for replacing the hip implant system or just the additional tests and monitoring that may be required. There will be cases where people are not required to have another hip replacement surgery but may have to subject themselves to endless monitoring, testing and uncertainty that their hip replacement system may fail at any other time. Other cases will be more severe and could include serious and ongoing pain, dislocations and other problems with the Stryker Rejuvenate and ABG II Hip Replacement Systems. And there will be cases where the recalled Stryker hip has already failed or is performing so poorly that you elect to have the hip implant replaced as soon as possible. There are certain questions that most Stryker hip recall lawsuits will have in common and seek to answer, such as the company's internal documentation about problems with the modular-neck stem line of hip replacement systems. Were there concerns about the use of metal components even before the hip implants were manufactured? Once you tell us about how the Stryker hip recall has affected you and what problems you have encountered we will be able to answer any questions you may have.

No Fees Unless We Collect for You

We will represent all persons involved in a Stryker Hip Recall lawsuit on a contingency basis, meaning there are never any legal fees unless we win compensation in your case. For a free no-obligation consultation please fill out our short online contact form and one of our Stryker Hip Recall lawsuit attorneys will contact you to answer any of your questions.

Stryker Lawsuits Set a Precedent

The Stryker hip recall is not the first of its kind; just two years ago, Stryker Orthopaedics recalled 93,000 hip replacement systems due to the metal parts' tendency to fret and corrode. Even before that recall was issued, there had been a number of lawsuits filed against the company over the problematic ASR line of hip replacement systems. Those lawsuits have alleged that Stryker Orthopaedics, Inc. manufactured a defective product, failed to warn patients and doctors of problems with the implant and negligence in designing, manufacturing and selling the product.


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