Olympus Corporation of the Americas recalls Uretero-reno fiberscope URF-P6
- Recall date
- January 17, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2519-2018
- FDA classification
- Class II
- Brand / firm
- Olympus Corporation of the Americas
- Sold / distributed
- US Nationwide. Canada and Mexico
Why it was recalled
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 fiberscope URF-P6
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