Olymp: Uretero-reno videoscope model URF-V2 may crack due to bending section issues. 1 unit recalled with serial number 2825505F.
The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
Olympus is recalling one unit of the URF-V2 uretero-reno videoscope because its bending section might crack, causing abnormal shape or angulation. This could affect medical procedures if the device malfunctions during use.
The bending section of the URF-V2 videoscope may crack under normal use, leading to an abnormal shape or angulation. This could cause the device to malfunction during medical procedures, potentially affecting the procedure's outcome.
Medical professionals who use this specific model for urological procedures are likely affected. The risk is low as only one unit was recalled and the issue involves potential bending section cracks rather than immediate harm.
Check for the model number URF-V2 on the device. The recalled unit has a specific serial number 2825505F and UDI 04953170343582.
Look for the model number URF-V2 on the device to confirm if it is the recalled unit.
Only 1 unit was recalled with serial number 2825505F.
The bending section may crack, resulting in abnormal shape or angulation.
The recall record does not specify a remedy.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1116-2022 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1116-2022 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.
