Olympus recalls GF-UCT180 ultrasound endoscopes due to updated cleaning instructions that may increase infection risk during use with diagnostic systems.
A new inspection step was added to the cleaning and disinfection section of the Instructions For Use (IFU) for this device in order to reduce the risk of causing patient infections.
Olymp: Olympus is recalling its GF-UCT180 ultrasound endoscopes because a recent update to cleaning instructions might increase infection risks during medical procedures. This affects healthcare providers using the device with specific diagnostic systems.
The updated cleaning instructions could lead to improper disinfection if not followed correctly, potentially increasing the risk of patient infections. This is a procedural risk rather than a physical hazard.
Healthcare providers who use Olympus GF-UCT180 ultrasound endoscopes with diagnostic systems like ALOKA CO. LTD equipment are most at risk. The recall applies to all units sold with these specific configurations.
Check for the model number GF-UCT180 on the device. The product is used with Olympus universal endoscopic ultrasound centers or diagnostic systems from ALOKA CO. LTD.
Check the device's Instructions For Use (IFU) for the updated cleaning steps to ensure proper disinfection.
The device is safe if cleaned according to the updated Instructions For Use (IFU).
The recall does not require immediate action; follow the updated cleaning instructions to reduce infection risk.
Look for the model number GF-UCT180 on the device, which is used with specific diagnostic systems like ALOKA CO. LTD equipment.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0500-2021 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0500-2021 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.
