Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0627-2018)

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 SM, Model Number 150802. 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-0627-2018

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: 28 devices

Code Information:

Model No. 150802: Lot No. 305330 (UDI (01)00880304240230(17)220506(10)305330), 305340 ((01)00880304240230(17)220506(10)305330), 305350 ((01)00880304240230(17)220517(10)305350), 356750 ((01)00880304240230(17)220523(10)356750).

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated