Class 1 Recall issued for the Zimmer Biomet Comprehensive Reverse Shoulder recalled by the FDA due to Serious Device Fractures
02/23/2017
class 1 recall issued for the zimmer biomet comprehensive reverse shoulder 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 ...
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