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Federal Judge Allows Stryker Hip Claim to Proceed

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A U.S. District Court Judge recently ruled to allow a Stryker hip implant lawsuit to continue after she dismissed two of the plaintiff’s claims, but allowed a claim regarding manufacturing defect to stand. In the lawsuit, the plaintiff alleged that he had suffered injuries and pain and was forced to undergo revision surgery after his Stryker Gamma3 Nail hip implant system failed.

Although the judge dismissed the strict liability design-defect and negligence claims against Stryker, the lawsuit’s strict liability manufacturing defect, breach of warranty, and loss of consortium claims will stand. The Gamma3 system is a metal on metal (MoM) hip implant, devices that have come under fire for causing a number of severe complications in patients.

Risks of Metal-on-Metal Hip Implants

All artificial hip implants carry risks including wear and tear of the component material, and MoM implants have unique risks in addition to the general risks of all hip implants:

 

According to the U.S. Food and Drug Administration (FDA), patients with a MoM hip implant may exhibit certain symptoms or illnesses elsewhere in the body. These include:

In April 2015, the FDA recommended that asymptomatic patients with MoM hip implants continue to follow-up with their orthopaedic surgeon every 1 to 2 years to monitor for early signs of change in hip status.

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