OMNIlife science Inc. recalls OMNI Hip System Model, Catalogue, or Order Number(s): HC-00
Recalled 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.
Hazard / Issue
Stems missing porous coating on the device.
Issued by
FDA
Affected States: OK, IL
Lot/Code Info: Lot # 33035
View official government recall
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