Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small
Reported: June 12, 2019 Initiated: April 18, 2019 #Z-1740-2019
Product Description
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small
Reason for Recall
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Details
- Recalling Firm
- Zimmer Biomet, Inc.
- Units Affected
- 14 units
- Distribution
- CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small. Recalled by Zimmer Biomet, Inc.. Units affected: 14 units.
Why was this product recalled? ▼
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 12, 2019. Severity: Moderate. Recall number: Z-1740-2019.
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