Olympus Corporation of the Americas recalls Olympus Pleuravideoscope, Model LTF-160
- Recall date
- March 23, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1762-2020
- FDA classification
- Class II
- Brand / firm
- Olympus Corporation of the Americas
- Sold / distributed
- US Nationwide
Why it was recalled
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Olympus Pleuravideoscope, Model LTF-160
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