Zimmer Biomet, Inc. recalls Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
- Recall date
- December 21, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0937-2019
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- MN, VA Foreign: Korea, New Zealand and Japan
Why it was recalled
Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
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 Series-A Standard Patella sizes 31mm Item Number: 184764
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