Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with… — Class II medical device recall Z-0972-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-03-13, distributed in AR, KY, WA. The product was potentially being packaged without a taper adapter.
| Recall number | Z-0972-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-12-21 |
| Classified | 2019-03-01 |
| Reported by FDA | 2019-03-13 |
| Terminated | 2020-05-06 |
| Distributed | AR, KY, WA |
| Countries outside the US | AU, JP |
| Quantity | 52 |
| Lot numbers | 921950, 994110 |
| Model numbers | 010000589 |
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.
Reason for recall
The product was potentially being packaged without a taper adapter.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0972-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.