Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial B
Recalled Product
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty
Hazard / Issue
The implant only has one bolt in the sterile package but it should have had two.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot 585070, UDI (01) 0088030448157 (17) 230215 (10) 585070
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