medical Class II Updated 2019-06-12

Zimmer Biomet, Inc. recalls Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral D

Recalled Product

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420321 Phase 3 Femoral Drill Guide Small


Hazard / Issue

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Issued by

FDA

Affected States: CA, IN, LA, NM, NY, TX, WI
Lot/Code Info: Lot Numbers: ZB160201 ZB160401 ZB161101 ZB170401 ZB170601 ZB170801 ZB170901
View official government recall

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