Biomet Orthopedics Intramedullary Bone Saw Cam Assembly… — Class II medical device recall Z-0594-2020
Terminated recall by Zimmer Biomet, Inc., reported 2019-12-11, distributed in CA, FL, IN, MN, MO, NY, UT. Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Ass
| Recall number | Z-0594-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-10-25 |
| Classified | 2019-12-03 |
| Reported by FDA | 2019-12-11 |
| Terminated | 2020-04-30 |
| Distributed | CA, FL, IN, MN, MO, NY, UT |
| Countries outside the US | AU, NZ |
| Quantity | 26 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00880304386570 |
| Lot numbers | 025800, 025810, 081640 |
| Model numbers | 475660 |
Product
Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Reason for recall
Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam
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-0594-2020. 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.