Biomet Oxford recall
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large
Why was Biomet Oxford recalled?
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: ZB161102 ZB170201 ZB170301 ZB170401 ZB170901
- Product
- Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 11 units
- Distribution
- CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS
- Recall date
- June 12, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)