Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide Small
Reported: June 12, 2019 Initiated: April 18, 2019 #Z-1741-2019
Product Description
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide 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
- 15
- 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: 32-421930 System Domed Lateral Femoral Drill Guide Small. Recalled by Zimmer Biomet, Inc.. Units affected: 15.
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-1741-2019.
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