Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0628-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty.

Product Classification:

Class II

Date Initiated: August 25, 2017

Date Posted: February 21, 2018

Recall Number: Z-0628-2018

Event ID: 79095

Reason for Recall:

The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension.

Status: Terminated

Product Quantity: 11 devices

Code Information:

Model No. 150804: Lot No. 088080 ((01)00880304240247(17)220606(10)088080), 305410 ((01)00880304240247(17)220601(10)305410).

Distribution Pattern:

US Nationwide Distribution to IN, MO, NY, TX.

Voluntary or Mandated:

Voluntary: Firm initiated