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Zimmer Biomet, Inc. recalls Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Recalled March 21, 2018 · FDA recall Z-1011-2018 · Zimmer Biomet
Hazard
The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur. · FDA Class II
Units
8
Sold at
US Distribution to states of: FL, WI, MD, MO, and MI.
Description
The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
Product
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →