Olympus recalls specific GIF-HQ190 gastrointestinal videoscopes due to potential image loss and suction issues that could delay treatment or cause infections.
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
Olympus is recalling certain GIF-HQ190 gastrointestinal videoscopes because a repair might cause image loss or suction problems. This could lead to delayed treatment or infection risks for patients.
The light guide connector may not be properly secured due to missing adhesive, causing image loss or suction issues. This could delay medical treatment or expose patients to infections.
Healthcare providers using the recalled models are most at risk, particularly those in settings where timely procedures are critical.
Check for serial numbers 2270393, 2201027, 2201611, or 2745407 on the device. The product is sold under the brand name Olympus.
Look for the serial numbers 2270393, 2201027, 2201611, or 2745407 on the videoscope.
Reach out to Olympus directly for further instructions on the recall.
The recall is due to a potential issue with the light guide connector repair that could cause image loss or suction problems, leading to delayed treatment or infection risks.
Check the serial number against the listed numbers (2270393, 2201027, 2201611, 2745407) and contact Olympus for instructions.
The recall states it could lead to delayed treatment or patient exposure to contaminated material, but does not specify serious injury risks.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0417-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0417-2024 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.
