High Fracture Rate – Zimmer Biomet Shoulder Replacement Device

Zimmer Biomet Shoulder replacement device was found to have a higher risk of fracturing than it was earlier believed, consumers at risk.

Labeling of the Zimmer Biomet Shoulder replacement failed to adequately disclose fracture risks. Those who received the shoulder replacement may experience substantial pain and suffering.

The Biomet Comprehensive Reverse Shoulder recall, was issued as Class I. Class I recalls are reserved for some of the most serious recalls issued by FDA.  

Risks include:

  • Death
  • Infection
  • Loss of shoulder movement

In December, Zimmer Biomet sent a recall notice and a Certificate of Acknowledgement to all affected customers.

Those with adverse events or side effects related to the use of these products are urged to report such problems.

If you or a family member have received the Biomet Comprehensive Reverse Shoulder System Humeral Tray Model 115340, you may be entitled to compensation. Connect with an attorney at Medical Claim Legal.