In December of 2016, Zimmer Biomet issued a medical device recall on thousands of devices used in patients from 2008 through 2015. The Zimmer Biomet Shoulder Replacement device is supposed to restore shoulder movement and help patients, but the reverse shoulder replacement device fractures at a higher rate than was reported to the public. The FDA issued a Class I recall on the device in 2017.
We are currently pursuing cases in which an individual had a Zimmer Biomet shoulder replacement that fractured, failed, or required a revision of the shoulder replacement. Goldenberg Heller & Antognoli has more than 30 years of legal experience to protect our clients and win them the compensation they deserve.
Our Approach to Zimmer Biomet Claims
Zimmer Biomet Device fractures may cause a variety of issues, including:
- Device breakage
- Severe pain
- Loss of shoulder function
- Replacement surgery
If you or a loved one have experienced any of these issues, contact your treating physician immediately to determine if a Zimmer Biomet device was used.
Free Zimmer Biomet Claims Consultation
We assist Zimmer Biomet clients in Illinois, Missouri and across the country. We are ready to discuss your legal options.
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