Olympus recalls ENF-GP2 Rhino-Laryngo Fiberscopes with serial numbers listed. Products repaired using incorrect service manuals may have missing O-rings, risking rework issues. Affected users should contact Olympus for details.
Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.
Olympus is recalling specific models of Rhino-Laryngo Fiberscopes due to a risk that improper repairs could cause missing O-rings. This could lead to rework issues if the device is used incorrectly. The recall affects users who have the listed serial numbers.
Products repaired with the incorrect service manual may be missing an O ring. This could cause rework issues if the device is used after repair, potentially leading to improper function.
Users of the ENF-GP2 Rhino-Laryngo Fiberscope with the listed serial numbers are affected. Medical professionals using the device for nasal and nasopharyngeal procedures are most at risk.
Check the serial number on your ENF-GP2 Rhino-Laryngo Fiberscope. The affected units have specific serial numbers listed in the recall notice.
Look for the serial number on your device to confirm if it is in the list of affected units.
Products repaired with the incorrect service manual may be missing an O ring, which could lead to rework issues.
Check the serial number against the list provided in the recall notice. Contact Olympus for further instructions.
The recall indicates a risk of rework issues if the device is repaired incorrectly, but there is no mention of immediate safety hazards.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2292-2020 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2292-2020 from Olympus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
