Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1738-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large

Product Classification:

Class II

Date Initiated: April 18, 2019

Date Posted: June 12, 2019

Recall Number: Z-1738-2019

Event ID: 82818

Reason for Recall:

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

Status: Terminated

Product Quantity: 11 units

Code Information:

Lot Numbers: ZB161102 ZB170201 ZB170301 ZB170401 ZB170901

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated