Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill… — Class II medical device recall Z-1739-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-06-12, distributed in CA, IN, LA, NM, NY, TX, WI. Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potential
| Recall number | Z-1739-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-04-18 |
| Classified | 2019-06-06 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-09-10 |
| Distributed | CA, IN, LA, NM, NY, TX, WI |
| Countries outside the US | AU, CA, JP, NL |
| Quantity | 3 units |
| Lot numbers | ZB110301 |
| Model numbers | 32-420324PHASE |
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large
Reason for recall
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
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-1739-2019. 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.