The FDA has issued recalls on several Zimmer NexGen knee replacements. In addition to the recalled products, there are more Zimmer NexGen knee replacement components which are under FDA investigation. These FDA knee implant recalls and investigations have been done as a result of possible defective product designs of Zimmer NexGen knees.
Patients who have had knee implants of these potentially defective knees, may have of loosening of the knee or early failure. This may lead to the need for a knee revision surgery.
Bernheim & Dolinsky, L.L.C., are reviewing potential lawsuits for individuals who have received certain components, including:
- Zimmer NexGen LPS
- Zimmer NexGen CR-Flex
- Zimmer NexGen MIS Tibial
Current Product Liability Claims
|Actos||DePuy ASR Hip Implant||Avaira Contact Lenses|
|Denture Cream Claims||Zimmer Durom Cup Hip Replacement||Medtronic Infuse Bone Graft|
|Shoulder Pain Pumps||Stryker Hip Implant||Transvaginal Mesh Implant|
|Zimmer NexGen Knee Implant|
More dangerous medical devices
For more information please contact Bernheim & Dolinsky, L.L.C. at 1-800-474-4089 or contact us online.
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