medical Class II Updated 2019-03-13

Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder System Glenosphere Mini Basep

Recalled Product

Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet Comprehensive Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthropathy and/or previously failed shoulder joint replacement with a grossly deficient rotator cuff.


Hazard / Issue

The product was potentially being packaged without a taper adapter.

Issued by

FDA

Affected States: AR, KY, WA
Lot/Code Info: Lot Numbers 994110, 921950 UDI Numbers: (01) 0 0880304 53246 5 (17) 280920 (10) 994110 (01) 0 0880304 53246 5 (17) 280913 (10) 921950
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