36MM COCR MODULAR HD -6MM — Class II medical device recall Z-1008-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-03-21. One piece from a different lot mixed with lot 236840 and is incorrectly etched as -6MM offset instead of +3MM
| Recall number | Z-1008-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-09-15 |
| Classified | 2018-03-14 |
| Reported by FDA | 2018-03-21 |
| Terminated | 2018-08-20 |
| Quantity | 23 |
| UPC / GTIN / UDI-DI | 00880304210509 |
| Lot numbers | 236840 |
Product
36MM COCR MODULAR HD -6MM
Reason for recall
One piece from a different lot mixed with lot 236840 and is incorrectly etched as -6MM offset instead of +3MM offset. As the incorrect etching and related size difference affects the functional use of this product, the affected lot is being removed from the field.
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-1008-2018. 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.