Stryker® Orthopaedics Hip Implant Recall

Stryker® Orthopaedics has voluntarily recalled its Rejuvenate modular and ABG-II modular-neck hip stem implants, according to the Food and Drug Administration (FDA). Stryker indicates that fretting and corrosion (wear and tear) can occur within the devices, which can cause adverse tissue reactions and pain and swelling in certain individuals.

While the hip socket joint in these models is not a metal-on-metal joint, there is a metal-on-metal joint within the workings of the recalled devices capable of deteriorating over time. As a result, certain recipients of these implants may experience the dangerous effects of Metallosis, which is a buildup of metal debris in the body’s soft tissues.

Hospitalization and painful corrective surgeries are sometimes necessary to alleviate pain and swelling caused by the affected Stryker implants. The company is urging those experiencing pain or swelling in their hip region to make an appointment with their surgeons to discuss their symptoms.

You May Be Entitled To Compensation

If you or someone you know received a recalled Stryker Orthopaedics hip implant and suffered painful swelling or related side effects that resulted in hospitalization or a revision surgery, contact a Stryker defective product lawyer using our free initial consultation form today. We may be able to help you get the compensation that you deserve for your hip replacement injury.

Which Implants Have Been Recalled?

Stryker Orthopaedics manufactures numerous medical implant devices. The devices targeted by this specific recall are the:

  • Rejuvenate Modular Hip System
  • ABG II modular-neck hip stem

You can verify the model of the hip implant that you received through a review of your medical records or a conversation with your surgeon.

Serious Health Risks

Recipients of recalled Stryker hip implants should consult their surgeons immediately if they experience pain or swelling in the area of their hip replacement. While fretting and corrosion are not outwardly visible due to the internal nature of an implant, these physical side effects can often be indicators that your particular hip replacement is defective. In certain cases, a painful revision surgery is necessary to correct health issues related to the recalled Stryker implants.

Stryker® is a registered trademark of Stryker Corporation. This law firm is not associated with, sponsored by, or affiliated with the U.S. Food and Drug Administration or Stryker Corporation.






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