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Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet C
Recalled March 13, 2019 · FDA recall Z-0972-2019 · Zimmer Biomet
Hazard
The product was potentially being packaged without a taper adapter. · FDA Class II
Units
52
Sold at
US Distribution to states of:: AR, KY, and WA.; Internationally to: Australia and Japan.
Description
The product was potentially being packaged without a taper adapter.
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.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →