# FDA recall Z-1739-2019

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-04-18.

## 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.

## Distribution

CA, IN, LA, NM, NY, TX, WI  Foreign: CANADA,  AUSTRALIA, JAPAN, NETHERLANDS

## Key facts

- **Recall number:** Z-1739-2019
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-18
- **Report date:** 2019-06-12
- **Termination date:** 2020-09-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1739-2019

## Citation

> AI Analytics. FDA recall Z-1739-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1739-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*