Olympus recalls LTF-S190-5 endoscopy videoscopes due to reprocessing instructions error. Affected units may cause improper cleaning if not followed correctly.
Instructions for Use-User Deviations related to the reprocessing of the videoscope detailed in the Reprocessing Manual Instructions. The steps are required for the proper reprocessing of these videoscopes
Olymp: Olympus is recalling its LTF-S190-5 endoscopy videoscopes because improper reprocessing could lead to contamination. This affects surgeons and medical staff using the device during procedures.
The videoscope requires specific reprocessing steps to prevent contamination. If these steps are not followed correctly, the device may become contaminated during use, potentially leading to infection risks.
Surgeons and medical staff who use the Olympus LTF-S190-5 endoscopy videoscope during procedures are most at risk. The recall applies to all units sold with the specific model number.
Check for the model number LTF-S19:5 on the device or its packaging. The device is used with video systems for endoscopic surgery in the thoracic and abdominal cavities.
Review the Reprocessing Manual Instructions for proper cleaning steps to avoid contamination.
The recall is for proper reprocessing to prevent contamination, but it does not pose an immediate risk if instructions are followed correctly.
The affected model is LTF-S190-5 with a 5.4 mm diameter. Check the device or packaging for this model number.
Follow the Reprocessing Manual Instructions to ensure proper cleaning and avoid contamination risks.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0644-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0644-2024 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.
