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Zimmer Biomet, Inc. recalls AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Ar
Recalled February 21, 2018 · FDA recall Z-0627-2018 · Zimmer Biomet
Hazard
The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension. · FDA Class II
Units
28 devices
Sold at
US Nationwide Distribution to IN, MO, NY, TX.
Description
The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension.
Product
AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →