Stryker Hip Implant Recall Attorney
Legal Expertise for Patients with Recalled Stryker Hip Implants
- Do you or a loved one have a recalled Stryker Hip Replacement Implant?
- Have you experienced unexplained pain and swelling?
In July 2012, Stryker Orthopaedics recalled its Rejuvenate Modular Hip System, which includes both Stryker’s Rejuvenate Modular and ABG II modular-neck hip stems. The company cited "potential risks associated with fretting and corrosion at the modular neck junction" as the reason for the recall.
If you or someone you care about is a recipient of either of these hip replacement systems, you need to know that the so-called "potential risks" have been found to be the cause of unexplained pain, tissue damage and swelling when the metal-on-metal components corrode.
The product liability specialists at Lowe Eklund Wakefield & Mulvihill Co., LPA (LEWM) carry special expertise in protecting the rights of patients affected by harmful surgical implants. Ranked by U. S. News & World Report on its "Best Law Firms" list three years running (2010-2012), LEWM is your best advocate for recourse.
We approach each client with singular dedication and treat every case like our most important case. If you think you’ve been hurt by one of the recalled Stryker hip components, call or e-mail our law firm today to schedule a no-obligation consultation for immediate help.