BIOMET ZipTight — Class II medical device recall Z-0212-2026
Ongoing recall by Biomet, Inc., reported 2025-10-29. There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Sin
| Recall number | Z-0212-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2025-09-23 |
| Classified | 2025-10-17 |
| Reported by FDA | 2025-10-29 |
| Quantity | 98 units |
| UPC / GTIN / UDI-DI | 00880304478404 |
| Lot numbers | 0002587666 |
| Model numbers | 904834 |
Product
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Reason for recall
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
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-0212-2026. 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.