AVID Medical, Inc. recalls PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.
- Recall date
- June 11, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2260-2025
- FDA classification
- Class II
- Brand / firm
- AVID Medical, Inc.
- Sold / distributed
- Domestic: CA, IL, MD, OH, PA, TX, WA.
Why it was recalled
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.
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