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Olympus Corporation of the Americas recalls Olympus Pleuravideoscope, Model LTF-240
Recalled April 29, 2020 · FDA recall Z-1763-2020 · Olympus Corporation of the Americas
Hazard
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided. · FDA Class II
Units
265 total
Sold at
US Nationwide
Description
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
Product
Olympus Pleuravideoscope, Model LTF-240
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →