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Zimmer Biomet, Inc. recalls Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
Recalled November 28, 2018 · FDA recall Z-0495-2019 · Zimmer Biomet
Hazard
Label on the outer carton or the patient labels does not match label on the inner sterile packaging · FDA Class II
Units
8 units
Sold at
AR, MO, MN, NJ, NY, OH, MN , NJ, VA
Description
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Product
Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →