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Zimmer® Hip Implants Attorneys Jacksonville

FDA Recall, Warning or Action: Zimmer Holdings, Inc. initiated a voluntary U.S. recall of the Durom Cup hip implant in 2008 because of complaints about device failures resulting from loosened components.

Healthcare providers and patients alike trust industry leaders to manufacture new medical products in the best interest of the general public. Our in-house team members routinely scrutinize the favorable rulings handed down by the courts for cases related to negligent medical devices. To learn more about metal-on-metal hip failures, visit our Dangerous Drugs page.

Side Effects of Zimmer® Hip Implants Use

Zimmer® hip implant construction reduces the risk of hip dislocation and preserves more of the hip joint’s natural cavity. The manufacturer warns that benefits must be weighed against the surgical skill required to successfully perform the procedure. Possible ill effects or negative patient outcomes include:

  • Loosening of Implants
  • Chronic Pain & Inflammation
  • Inadequate Fixation Surface
  • Implants Not Fully Seating
  • Metallosis Poisoning
  • Post Implant Surgeries

NOTE: Failure rates for Zimmer® hip implants have been estimated as high as 30 percent within a few years from the time of hip replacement surgery.

Our lawyers may choose to work directly with other accomplished medical products law firms to assure adequate restitution for our injured clients and their families. If you lost a loved one or suffered severe injuries due to a dangerous or failed device, contact us at 904-251-1111 or 1-800-251-1111 for a FREE initial consultation.

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