Wet-Field Hemostatic Eraser Bipolar recalled over labeling errors
- Recall date
- February 26, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Beaver-Visitec International Inc. recalls Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
- Recall number
- Z-1801-2018
- FDA classification
- Class II
- Brand / firm
- Beaver-Visitec International Inc.
- Sold / distributed
- US Nationwide and Canada
Why it was recalled
Products were packaged with incorrect labeling,
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
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