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.
These devices are fracturing at a higher rate
than is stated. Revision surgeries may cause
serious adverse health consequences.