Have you suffered from Stryker Rejuvenate recall hip problems related to the July 2012 Stryker Rejuvenate recall and ABG II hip stem recall? The Stryker Rejuvenate and ABG II hip replacement devices were pulled from the market after it became apparent that the metal hip stems were likely to fret and corrode at the modular neck junction, putting patients at risk for pain, swelling, adverse local tissue reactions, and other painful problems. Even after Stryker Rejuvenate recall hip revision surgery to remove and replace the implants, many patients continue to suffer from debilitating Stryker Rejuvenate recall hip replacement problems due to the damage caused by metal ions shed from the defective Rejuvenate and ABG II stems.

Filing A Stryker Rejuvenate Lawsuit Or Stryker Rejuvenate Class Action Lawsuit

Victims of Stryker Rejuvenate hip recall problems associated with the Rejuvenate and ABG II components may be entitled to significant financial compensation for their pain and suffering. Wright & Schulte LLC, an experienced law firm focused on obtaining justice for the people, continues to offer free Stryker Rejuvenate hip recall lawsuit evaluations to victims of the Stryker Rejuvenate hip implant recall. To discuss compensation for your Stryker hip recall problems with a qualified personal injury lawyer, please contact Wright & Schulte LLC today.

Stryker Rejuvenate Recall FDA – Stryker Rejuvenate Hip Recall And ABG II Hip Recall

Stryker’s Rejuvenate and ABG II hip stems have a modular design that offered surgeons the option to choose components of various sizes, so that the hips could be custom fit to each individual patient. The hip stems were introduced to the market in 2009, and approved by the U.S. Food & Drug Administration (FDA) through a clearance process known as 510(k). This system allows a medical device to come to market without human testing when it is similar in design to a product that has already been approved by the FDA. As a result, the risk of Stryker hip problems associated with the Rejuvenate and ABG II stems did not become apparent until they had been implanted in thousands of people.

Stryker Rejuvenate Hip Recall Problems

Many of problems seen in Stryker hip recall patients are the result of microscopic metal ions that are shed from the hip stems when they fret or corrode. These minute particles can accumulate in the tissue surrounding the hip, as well as the blood stream, leading to any number of serious Stryker hip replacement problems, including:

  • Metallosis: A rare condition that is caused by the buildup of metallic debris in the soft tissue of the body
  • Osteolysis: The loss of bone around the hip. Osteolysis is the most common hip replacement complication, and has been named as the cause of nearly 75 percent of all hip implant failures
  • Necrosis or tissue death
  • Loosening and dislocation of the implant
  • Fracture of the implant
  • Device failure requiring revision surgery

Stryker has advised all Rejuvenate and ABG II hip recipients to undergo blood tests for metal ion levels and imaging screening, even if they are not experiencing any apparent Stryker hip recall problems. According to the company, some patients implanted with these components have tested positive for elevated metal ions and adverse local tissue reactions, even in the absence of symptoms.

Legal Options For Victims Of Stryker Rejuvenate Hip Recall Problems

If you or a loved one has suffered from Stryker Rejuvenate hip recall problems related to the Rejuvenate and ABG II hip stem recall, and you’re looking for a personal injury law firm that will guarantee the caring, personalized and loyal representation you deserve, please do not hesitate to contact Wright Schulte LLP today. For a free, no obligation Stryker Rejuvenate hip recall lawsuit evaluation, simply fill out the online form on the right, or give Wright & Schulte LLC a call, toll-free, at 1-800-399-0795.


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