Central Screw 6 — Class II medical device recall Z-1131-2021
Terminated recall by Biomet, Inc., reported 2021-02-24, distributed nationwide. Zimmer Biomet is conducting a lot specific medical device recall for the Comprehensive Reverse Shoulder Centra
| Recall number | Z-1131-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2021-01-15 |
| Classified | 2021-02-17 |
| Reported by FDA | 2021-02-24 |
| Terminated | 2023-03-09 |
| Distributed | Nationwide (US) |
| Quantity | 49 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00880304677074 |
| Lot numbers | 077170 |
| Model numbers | 115395 |
Product
Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
Reason for recall
Zimmer Biomet is conducting a lot specific medical device recall for the Comprehensive Reverse Shoulder Central Screw, 25 MM Length. It has been determined through a complaint investigation that a 40 MM length central screw was packaged and labeled as a 25 MM length central screw.
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-1131-2021. 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.