Olympus recalls EVIS EXERA III Gastrointestinal Videoscopes (GIF-1TH190) due to unclear drying procedures identified in human factors testing. Affected units have serial numbers less than 2446103.
To better define the drying procedures described in the IFU to improve the instructions for easier understanding of each drying step after human errors and concerns were identified when completing a Human Factors evaluation of the GIF-1TH190.
Olympus is recalling its EVIS EXERA III Gastrointestinal Videoscopes (model GIF-1TH190) because drying instructions were unclear after human factors testing found errors. This recall addresses potential confusion in following proper drying steps, which could lead to improper use.
The recall stems from human factors testing that identified errors in the drying procedures described in the user manual. This could lead to confusion about how to properly dry the videoscope after use, potentially causing improper handling or maintenance.
Users of Olympus EVIS EXERA III Gastrointestinal Videoscopes with model number GIF-1TH190 and serial numbers less than 2446103 are affected. Medical professionals performing endoscopy procedures are most at risk.
Check for the model number GIF-1TH190 on the device. Affected units have serial numbers less than 2446103. The product was sold by Olympus Corporation of the Americas.
Look for the serial number on the device; affected units have numbers less than 2446103.
Olympus identified errors in the drying procedures described in the user manual after human factors testing, which could lead to confusion in following proper drying steps.
Check the serial number; if it is less than 2446103, contact Olympus for further instructions.
The recall addresses potential confusion in drying procedures, but there is no indication of immediate injury risk. The hazard level is low risk.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0498-2025 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0498-2025 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.
