ZIMMER BIOMET COMPREHENSIVE SHOULDER IMPLANT RECALL 

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The defective medical device attorneys at The Carlson Law Firm are currently investigating potential lawsuits for individuals across the United States who have suffered health consequences due to the a Zimmer Biomet Comprehensive Shoulder Implant.

Claims have been filed against Zimmer Biomet because their Comprehensive Reverse Shoulder Humeral implant has been failing at a rate higher than the company expected or reported to the public.

  • ABOUT ZIMMER

    Zimmer Biomet is the second-largest medical device manufacturer in the world, each year selling more than 1 million artificial knee, shoulder, hip, ankle, foot and elbow implants.

  • RECALL HISTORY

    On Dec. 20th, 2016 Zimmer instituted a Class I recall of one of its most popular shoulder implant devices, the Comprehensive Reverse Shoulder. The recall was made after the implant was found to fracture at rates higher than expected.

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    COMMZON INJURIES

    Device fractures may cause device breakage, separation, severe pain, the loss of shoulder function, need for replacement surgery, infection or even death.

  • WHO IS ELIGIBLE?

    If you underwent shoulder replacement or implant surgery from 2008 to 2016 in which the Zimmer Biomet device was used, you may be eligible to file a claim for compensation.

  • History of Success, How We Can Help

    HOW WE CAN HELP

    Our defective medical device attorneys at The Carlson Law Firm can review your medical records to determine if you received the defective device.


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