Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 63x 10mm Universal Tibial
Recalled Product
Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 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 320390, UDI (01) 0088030448157 (17) 230129 (10) 320390
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