High Fracture Rates Lead to Recall of Zimmer Biomet Comprehensive Reverse Shoulder
Zimmer Biomet has initiated an urgent recall of its Comprehensive Reverse Shoulder due to high fracture rates. While this shoulder replacement device is intended to help restore arm movement, the FDA indicates that when the Comprehensive Reverse Shoulder fractures, individuals may require “revision surgeries which could cause serious adverse health consequences such as permanent loss of shoulder function, infection, or rarely, death.” Given these substantial risks, the FDA has identified this as a Class I recall, which is the most serious type of recall.
If you or a loved one suffered injuries that you believe were caused by Zimmer Biomet’s Comprehensive Reverse Shoulder, please contact one of the experienced medical device attorneys at Burg Simpson today. Our award-winning lawyers would be happy to discuss your potential claim. Call 1-800-713-9340 or fill out our contact form for a FREE no-obligation consultation today.