Olympus recalls two ultrasonic bronchoscopes due to potential water contamination in the channel after repair, risking infection. Affected models BF-UC180F and BF-UC190F sold in specific regions.
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 two specific ultrasonic bronchoscopes because water can remain in the channel after repair, creating a risk of infection. This affects medical devices used for airway procedures.
The channel air drying process wasn't properly validated, so some scopes returned after repair had water left behind. This water could cause contamination and lead to infection risks during medical procedures.
Healthcare providers using the specific Olympus bronchoscope models BF-UC180F and BF-:UC190F are most at risk. Patients receiving procedures with these devices could also be affected.
Check for model numbers BF-UC180F or BF-UC190F on the device. These models were sold with specific UDI-DI numbers: BF-UC180F (04953170356360) and BF-UC190F (04953170399831).
Look for model numbers BF-UC180F or BF-UC190F on the device.
The channel air drying process wasn't validated, so some scopes returned after repair had water left behind, creating infection risks.
Models BF-UC180F and BF-UC190F with specific UDI-DI numbers: BF-UC180F (04953170356360) and BF-UC190F (04953170399831).
Check for model numbers BF-UC180F or BF-UC190F on the device. These models were sold with specific UDI-DI numbers.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0328-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0328-2024 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.
