Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with… — Class II medical device recall Z-1208-2015
Terminated recall by Biomet, Inc., reported 2015-03-04, distributed in AL, FL, NY, TX. The taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minute
| Recall number | Z-1208-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2015-01-07 |
| Classified | 2015-02-24 |
| Reported by FDA | 2015-03-04 |
| Terminated | 2015-10-22 |
| Distributed | AL, FL, NY, TX |
| Lot numbers | 527400 |
| Model numbers | 010000589 |
Product
Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
Reason for recall
The taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minutes.
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-1208-2015. 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.