Smith Nephew Oxinium Knee Implants Recalled, Faulty
Last Updated on June 26, 2017
Investigation Complete
Attorneys working with ClassAction.org have finished their investigation into this matter. Check back for any potential updates. You can also sign up for our free newsletter for the latest in class action news and settlements.
If you still have questions about your rights, contact an attorney in your area as there is a time limit for filing all lawsuits. The information on this page was posted when the investigation began and is now for reference only.
Free Consumer Tools:
- Open and Current Class Action Lawsuit Settlements and Rebates
- Open and Current Class Action Lawsuit List, Investigations
- Class Action Lawsuit and Settlement News
- Free Class Action Lawsuit Database
At A Glance
- This Alert Affects
- Any patient fitted with Oxinium Genesis II or Profix II implants.
- Damages
- Muscle damage or infection from improper bonding.
- Company(ies)
- Smith Nephew
- Additional Details
- Revision surgery may be required in certain cases.
- Date
- Recalled in 2003
Smith Nephew, the makers of Oxinium Knee Implants, have issued a voluntary recall of selected Oxinium Genesis II and Profix II knee implants, admitting that they do not bond as intended. This could potentially lead to joint or muscle damage, increase chances of infection, and require revision surgery.
The cementless versions of the Oxinium Genesis II and Profix II were recalled in 2003 after the device’s impaired bonding ability meant many patients had to have revision surgery for their knee implants. Knee replacement surgery remains one of the most commonly performed replacement surgeries in the U.S., following its introduction in the 1970s. Smith Nephew Oxinium devices were offered from January 2000 until recall in September 2003, and the affected cementless devices should no longer be used.
Before commenting, please review our comment policy.