Olympus recalls tracheal videoscopes (model LF-V) due to potential infection from water contamination in the channel after repair. Affected units may have wet channels that could lead to infection risks.
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 trache:al videoscopes (model LF-V) because water in the channel after repair could lead to infection. This risk occurs if the device is not properly dried after use, potentially causing contamination.
The channel air drying process wasn't validated, so some scopes returned after repair had water remaining. This water could cause contamination, leading to infection risks if the device is used without proper drying.
Healthcare professionals using the Olympus tracheal videoscope (model LF-V) are most at risk. Patients using these scopes for airway management could also be affected if the device is contaminated.
Check for the model number LF-V on the device. The product was sold with the UDI-DI code 04953170340246. This recall applies to scopes used for airway management.
Inspect the channel for water after use; if wet, contact Olympus for guidance.
The channel air drying process wasn't validated, so some scopes returned after repair had water remaining, which could lead to infection risks.
Check for the model number LF-V and the UDI-DI code 04953170340246 on the device.
Contact Olympus directly for guidance on how to handle the contaminated scope.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0339-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0339-2024 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.
