Zimmer Biomet is recalling 3,662 units of the Comprehensive Reverse Shoulder due to a higher rate of fracture occurrence than was stated in the labeling.
FDA has identified this as a Class I recall. Affected lot numbers were manufactured between August 2008 and September 2011, and distributed between October 2008 and September 2015. A notice sent to affected customers recommended no specific patient monitoring instructions, beyond existing surgical follow-up protocol.
Zimmer Biomet is recalling 3,662 units of the Comprehensive Reverse Shoulder due to a higher rate of fracture occurrence than was stated in the labeling.
FDA has identified this as a Class I recall. Affected lot numbers were manufactured between August 2008 and September 2011, and distributed between...
Zimmer Biomet is recalling 3,662 units of the Comprehensive Reverse Shoulder due to a higher rate of fracture occurrence than was stated in the labeling.
FDA has identified this as a Class I recall. Affected lot numbers were manufactured between August 2008 and September 2011, and distributed between October 2008 and September 2015. A notice sent to affected customers recommended no specific patient monitoring instructions, beyond existing surgical follow-up protocol.
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