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FDA Medical Device Report For The Oxinium Knee Implant
From March 2002 to November 2011 the FDA received more then 248 individual reports from people who had used the Oxinium Knee Implant.
Reported Events
Event Totals:
| Injury | 238 |
| Malfunction | 10 |
Complications of Oxinium Knee Implant:
Some of the complications experienced after using the Oxinium Knee Implant include:
Oxinium Knee Implant Injuries Associated with Many Brands:
Injuries have been associated with many manufacturers and brands including Journey, Oxinium, Journey Bcs, Journey Uni, Genesis Ii, Journey Deuce, Bcs Tibia Base Plate, Juni, Genesis Uni and Journey Guidewire.
Contact Our Defective Oxinium Knee Implant Product Lawyers:
A medical device lawyer represents the interests of those who have been harmed by or lost loved ones as a direct result of a dangerous medical device. A medical device attorney may represent an individual client or take part in a mass tort action. If you or a loved one were injured by the Oxinium Knee Implant medical device. Call toll free (866) 735-2792 to schedule a private, no-cost consultation with an attorney who can evaluate your claim and get your case started.