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FDAMay 5, 2020device

ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.

What to do

FDA enforcement status: Terminated

Brands named

olympus

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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