Olympus recalls Duodenovideoscope-EndoTherapy accessories (biopsy forceps, etc.) due to potential water contamination in the channel after repair, risking infection. Affected models include TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.
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 certain endoscopy accessories because water in the channel after repair could lead to infection. This affects specific models sold with unique serial numbers. If you own these items, contact Olympus for details.
Water remaining in the channel after repair can cause contamination. This contamination may lead to infections if the equipment is used without proper cleaning.
Endoscopy patients and healthcare providers using the recalled accessories. Those with the specific model numbers listed are most at risk.
Check for model numbers TJF-145, TJF-150, TJF-Q180V, or TJF-Q190V on the accessories. The serial numbers listed are also specific to these models.
Inspect the channel for water after use; if wet, stop using the accessory immediately.
Reach out to Olympus directly for instructions on returning or repairing the affected accessories.
The affected models are TJF-145, TJF-150, TJF-Q180V, and TJF-Q190V with specific serial numbers listed in the recall notice.
Check the model number on the accessory; if it matches TJF-145, TJF-150, TJF-Q180V, or TJF-Q190V, it may be affected.
The recall addresses infection risk from water contamination, not direct injury. Serious injury is not mentioned in the hazard description.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0346-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0346-2024 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.
