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...

document icon

You are out of free articles for this month

Subscribe as a Guest for $0 and unlock a total of 5 articles per month.

You are out of five articles for this month

Subscribe as an Executive Member for access to unlimited articles, THE ORTHOPAEDIC INDUSTRY ANNUAL REPORT and more.


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

Contact Us