Stryker Hip Replacement Failure Attorneys

The Nation's Leading Law Firm for Defective Stryker Hip Replacement Implants

Thousands of patients have experienced complications from a Stryker hip implant and have filed lawsuits after suffering through intense pain and revision surgery. Stryker recalled its Rejuvenate, ABG II and Accolade TMZF modular-neck hip stems after the implants showed signs of corrosion and fretting. The company's LFIT V40 Head is also speculated to cause the same issues.

Have you or a loved one suffered from complications to a Stryker hip device? Call us at (877) 285-7656 for a free case evaluation.

What Should I Do?

As new developments related to Stryker news occur, we will update our Stryker News section and communicate directly with our clients. If you have yet to begin your journey to get justice for your faulty hip, take the following steps to get started.

Contact Your Doctor

If you received a Stryker Hip implant and have been experiencing problems, contact your doctor immediately to discuss your symptoms and next steps.

Have Our Experts Review Your Case

Stryker has a duty to properly design their products and warn the public about any risks. The company has recalled a number of its hip implants and it may be too late for a number of people who received faulty implants. Have our qualified Stryker lawyer review your case and find out if you have a claim for compensation.

If you choose to file a lawsuit, you may be eligible for the following types of compensation:

  • Medical expenses
  • Compensatory damages
  • Pain & suffering
  • Loss of consortium
  • Punitive damages

See Our Attorneys

Stryker Hip Recalls

Stryker Rejuvenate

Recalled June 2012
Studies found that the device’s modular-neck junction was prone to fretting and corrosion mechanisms, causing the release of metal ions into the bloodstream and surrounding hip tissue.

Rejuvenate Recall Information

Stryker Accolade TMZF

Recalled July 2009
The Accolade stem, when implanted in conjunction with the L-Fit V-40 femoral head, operates as a metal-on-metal hip implant system. The metal was found to fret & corrode, causing the release of metal ions into the body.

Accolade TMZF Recall Information

Stryker LFIT V40

Recalled August 2016
Stryker notified it's implanting physicians of the "higher than expected" incidents of taper lock failure, or spontaneous dissociation. The metal-on-metal design is also prone to cause metal toxicity.

LFIT V40 Recall Information


Free Consultation

If you have undergone a hip replacement surgery and have been implanted with a defective Stryker medical device, you have likely heard about or received a letter outlining the nature of the different recalls.

If you’re unsure which device you have in your hip, call us. Our Stryker Recall Lawyers can look into the details at no cost to you and see if you qualify for a claim.