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How do I know if I have a recalled metal-on-metal hip implant?

NOTICE: The Drug Law Center is no longer accepting these type of cases. This page is strictly for informational purposes. We appreciate your cooperation and understanding by not contacting our office on these cases. We are actively investigating and prosecuting cases involving Valsartan cancers. For information on Valsartan lawsuits, look here.

In the United States, most medical device companies do not keep a formal record as to who are recipients of their products. Since the initiation of the recall, many orthopedic surgeons (who do keep an inventory of their patients) have sent letters to their patients who have devices implicated by the Stryker Rejuvenate Modular Hip System or the Stryker ABG II Modular-Neck Hip Stem recall.

However, even if you did not receive a notification from your physician or medical center where the surgery was performed—you may still have a device implicated by the recall. If you are unsure of the type of hip prosthesis that you have, you can contact the Stryker hip defect attorneys as Drug law Center to help determine if you are implicated by the recall.

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About the Drug Law Center

The Drug Law Center is sponsored by lawyers who represent individuals and families who have suffered a serious injury or death from a dangerous drug or medical device. While these medical inventions have been marketed to improve the quality of life for people, unsafe drugs and poorly designed medical devices can drastically reduce the quality of life for the individual and his or her family.

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