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Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in T
Recalled October 3, 2018 · FDA recall Z-3250-2018 · Zimmer Biomet
Hazard
The implant only has one bolt in the sterile package but it should have had two. · FDA Class II
Units
16
Sold at
Worldwide Distribution: US (nationwide) to the following US states: AZ, KS, NM, NV, and UT; and to countries of: Australia and Netherlands.
Description
The implant only has one bolt in the sterile package but it should have had two.
Product
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →