Zimmer NexGen Knee Implant

NexGen Knee Product Liability Claims

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

ActosDePuy ASR Hip ImplantAvaira Contact Lenses
Denture Cream ClaimsZimmer Durom Cup Hip ReplacementMedtronic Infuse Bone Graft
Shoulder Pain PumpsStryker Hip ImplantTransvaginal Mesh Implant
Zimmer NexGen Knee Implant

More dangerous medical devices

Artelon CMC SpacerAvaira Contact LensesBard IVC Filter
Denture CreamDePuy ASR Hip ImplantDePuy LPS Diaphyseal Sleeve
DePuy Pinnacle Utamet Hip ImplantMedtronic INFUSE Bone GraftShoulder Pain Pump
Stryker Hip ImplantTransvaginal MeshZimmer Durom Cup Hip Replacement
Zimmer NexGen Knee Implant
Medical Devices HomeProduct Liability Home

For more information please contact Bernheim & Dolinsky, L.L.C. at 1-800-474-4089 or contact us online.

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Product liability litigation has been featured on:

Bernheim & Dolinsky: American Association of Justice.
Bernheim & Dolinsky: Miami-Dade Justice Association. Bernheim & Dolinsky: Broward County Bar Association. Bernheim & Dolinsky: Broward County Justice Association.
Bernheim & Dolinsky: Million Dollar Associates Forum.