Comprehensive Reverse Shoulder Lawsuit
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 injuries.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious adverse health consequences such as permanent loss of shoulder function, infection, or rarely, death.
FDA Warning:
These devices are fracturing at a higher rate
than is stated. Revision surgeries may cause
serious adverse health consequences.
