Olympus Corporation of the Americas recalls Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
- Recall date
- January 17, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2518-2018
- FDA classification
- Class II
- Brand / firm
- Olympus Corporation of the Americas
- Sold / distributed
- US Nationwide and Canada
Why it was recalled
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
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