Help and information about Stryker Hip Replacement recalls.
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Stryker ABG II Modular Recall

When was the Stryker ABG II Modular recall issued? In June 2012, the Stryker Corporation announced a voluntary recall from the manufacturer for the ABG II Modular hip-replacement unit. A recall was also issued in Canada in May 2012. Why was the Stryker ABG II Module recalled? The Stryker ABG II Module was recalled due to health and safety concerns. Patients have experienced symptoms such as

  • pain
  • swelling
  • difficulty walking

These symptoms are linked to a number of potential problems with the Stryker ABG II, including:

  • fretting and corrosion
  • loosening
  • metal poisoning
  • bone fractures
  • dislocation

I’ve experienced problems with my Stryker ABG II hip implant. How do I know if I have a case? If you or a loved one has experienced Stryker hip replacement problems, contact the lawyers at Hissey Kientz, LLP to learn more about your legal rights. You can reach us by calling toll-free at 1-866-275-4454, or by filling out a free case evaluation form on the right of this page.

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