Zimmer Biomet, Inc. recalls Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
- Recall date
- October 22, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0495-2019
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- AR, MO, MN, NJ, NY, OH, MN , NJ, VA
Why it was recalled
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
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