Olympus recalls EVIS EXERA III Colon Videoscopes with 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.
Olymp: Olympus is recalling specific EVIS EXERA III Colon Videoscopes due to a repair issue that may cause image loss, reduced suction, or infection risks during procedures. This could lead to delayed treatments or patient exposure to contaminated materials.
The videoscope may have a light guide connector that wasn't properly secured with adhesive. This can cause image loss, reduced suction, or problems with reprocessing the device, potentially delaying treatment or exposing patients to infections.
Healthcare professionals using the EVIS EXERA III Colon Videoscopes for colonoscopies are most at risk. Patients undergoing procedures with these devices may face delays or infection risks.
Check for the model PCF-H190L or serial numbers 2302719 and 2516751 on the device. The recall applies to specific units sold by Olympus.
Verify the model number and serial number on the device to confirm if it is affected.
The videoscopes may have an improperly repaired light guide connector due to missing adhesive, which can cause image loss, reduced suction, or infection risks.
Check for the model PCF-H190L or serial numbers 2302719 and 2516751 on the device.
The recall does not specify a remedy, so contact Olympus directly for guidance.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0419-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0419-2024 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.
