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Olympus Corporation of the Americas recalls ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.
Recalled June 17, 2020 · FDA recall Z-2292-2020 · Olympus Corporation of the Americas
Hazard
Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual. · FDA Class II
Units
19
Sold at
US Nationwide distribution including in the states of FL, MI, NM, NY, OH, and OR. No international distribution.
Description
Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.
Product
ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →