Zimmer Biomet, Inc. recalls Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
- Recall date
- May 8, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2198-2017
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- Nationwide Worldwide
Why it was recalled
Durability characteristics of reusable instruments were not established
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
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