Medical Device Safety and Recalls: Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Medical Device Safety and Recalls: Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

Zimmer Biomet is recalling the Comprehensive Reverse Shoulder because these devices are fracturing at a higher rate than is stated in the labeling. Fractures may result in revision surgeries which could cause serious adverse health consequences such as permanent loss of shoulder function, infection, or rarely, death.

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