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OMNIlife science Inc. recalls OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primar
Recalled October 30, 2019 · FDA recall Z-0169-2020 · OMNIlife science
Hazard
Stems missing porous coating on the device. · FDA Class II
Units
3 units
Sold at
OK, IL
Description
Stems missing porous coating on the device.
Product
OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primary or revision total hip replacement.
Manufacturer(s)
OMNIlife science Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →