Olympus recalls certain ultrasonic gastrovideoscopes due to potential water contamination in the channel after repair, which could lead to infection. Affected models include TGF-UC180J with specific serial numbers.
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
Olympus is recalling specific ultrasonic gastrovideoscopes that may have water remaining in the channel after repair. This water could lead to infection if the device is used improperly.
The channel air drying process wasn't properly validated, so some scopes returned after repair had water left inside. This water could cause contamination during use, potentially leading to infections.
Healthcare professionals who use the recalled ultrasonic gastrovideoscopes for endoscopic procedures are most at risk. Patients using these devices could also face infection risks if the contamination occurs.
Check for model number TGF-UC18:0J on the device. The specific serial numbers are 04953170328480. These scopes were sold with the model number TGF-UC180J.
Inspect the channel for water residue after use. If water is present, stop using the device immediately.
The channel air drying process wasn't validated, so some scopes returned after repair had water left inside, which could lead to contamination and infection.
The affected model number is TGF-UC180J with serial number 04953170328480.
Check for model number TGF-UC180J on the device. The specific serial number 04953170328480 indicates the recalled unit.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0345-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0345-2024 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.
