Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635… — Class II medical device recall Z-2870-2026
Ongoing recall by Biomet, Inc., reported 2026-08-12. Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw B
| Recall number | Z-2870-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2026-07-01 |
| Classified | 2026-08-03 |
| Reported by FDA | 2026-08-12 |
| Quantity | 22 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00887868507823 |
| Lot numbers | 67818769, 67818770 |
| Model numbers | 475635 |
Product
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm
Reason for recall
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
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-2870-2026. 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.