Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate (FDA)
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Recalled Product:
Product Description: Comprehensive Reverse Shoulder System Humeral Tray Model 115340
Trade Name: Biomet Comprehensive Reverse Shoulder Humeral
Product Code: KWS, PAO
Lot Numbers: All lots with part number 115340; See full list of lot numbers
Distribution Dates: October, 2008 to September, 2015
Manufacturing Dates: August 25, 2008 to September 27, 20...
