Olympus recalls certain colonoscopes for potential infection risk from water contamination in the channel after repair. Affected models include PCF-H180AI and others sold in the U.S. from 2018 to 2020.
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 colonoscopes that could have water remaining in the channel after repair, which might lead to infection. This is a safety issue for patients using these devices during medical procedures.
The channel air drying process wasn't properly validated, so some scopes returned after repair had water left in the channel. This water could cause contamination and lead to infection if the scope is used again.
Patients who have received a colonoscopy using the recalled Olympus colonoscopes are most at risk. Healthcare providers using these models for medical procedures may also be affected.
Check if your colonoscope has model numbers like PCF-H180AI, PCF-H190DI, or PCF-Q180AI. These models were sold in the U.S. from 2018 to 2020.
Look for model numbers on the colonoscope, such as PCF-H180AI or PCF-H190DI.
Reach out to Olympus for guidance on whether your colonoscope is affected and next steps.
The channel air drying process wasn't validated, so some scopes returned after repair had water in the channel, which could lead to infection.
Check the model number on your colonoscope. Affected models include PCF-H180AI, PCF-H190DI, and others listed in the recall notice.
Contact Olympus directly to determine if your colonoscope is affected and follow their instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0341-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0341-2024 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.
