If you suffered complications after receiving a Stryker Hip Implant, we can help.

Stryker Hip systems are releasing toxic, metal ions into the surrounding tissue.

The medical device attorneys of Elk & Elk are investigating cases involving patients who have suffered pain and discomfort as a result of a Stryker Hip implant. On July 4, 2012, Stryker issued a recall of its Rejuvenate Modular Primary Hip System and Rejuvenate Total Hip System due to possible side effects similar to those seen in metal-on-metal hip implants.

The Stryker Modular Hip replacement system has been linked to serious complications, including:

  • Fretting (wear) and/or corrosion at the modular-neck junction possibly leading to osteolysis (bone dissolution)
  • Joint loosening/dislocation stryker
  • Multi-organ injuries from the release of heavy metals into the body
  • Tissue inflammation
  • Necrosis (soft tissue death)
  • Hypersensitivity/allergic response
  • Broken devices
  • General pain and discomfort

Any of the symptoms above may indicate that revision surgery is required.

If you or a loved one suffered from any of these complications after receiving a Stryker Hip implant, you need to contact us today. Simply fill out the contact form on this page and find out how we can help you. You can also always reach us 24/7/365 at 1-800-ELK-OHIO.