FDA Device recall Z-1739-2019
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large
- FDA Device
- Class II
- terminated
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large by Zimmer Biomet, citing incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1739-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-18 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | CA, IN, LA, NM, NY, TX, WI |
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large
Reason
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Identifiers
| code_info | Lot Numbers: ZB110301 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1739-2019%22
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