Olympus recalls GIF-H180J gastrointestinal videoscopes due to potential adhesive repair issues affecting durability. Owners should contact Olympus for details.
The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
Olympus is recalling its GIF-H180J gastrointestinal videoscopes because the adhesive used in repairs might not hold properly. This could lead to the scope failing during use, but the exact risk isn't clear.
The adhesive used in repairs was prepared incorrectly, which may cause the repair to fail. This could lead to the endoscope breaking during use, potentially causing injury or complications. However, the exact impact on safety is not specified.
Healthcare professionals using Olympus GIF-H180J endoscopes for gastrointestinal procedures are most at risk. Patients using these scopes under medical supervision are also affected.
Check for the serial number 2418319 on the Olympus GIF-H180J gastrointestinal videoscope. These scopes were sold for endoscopic procedures in the gastrointestinal tract.
Reach out to Olympus Corporation of the Americas for specific guidance on the recall and next steps.
The recall states the adhesive repair might not hold properly, but the exact risk is unknown. Olympus has not confirmed if the product is safe.
Check for the serial number 2418319 on the Olympus GIF-H180J gastrointestinal videoscope.
Olympus has not provided a specific remedy, so contact them directly for instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1008-2019 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1008-2019 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.
