Zimmer Biomet Recalls Comprehensive Reverse Shoulder

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...

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JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



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