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FDAApril 20, 2022device

Olympus URETERO-RENO FIBERSCOPE Model: URF-P6

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision and unintentional contact with the patients body and in rare cases perforation in the urinary tract/renal pelvis.

What to do

FDA enforcement status: Ongoing

Brands named

olympus

UPCs

04953170340802

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Olympus URETERO-RENO FIBERSCOPE Model: URF-P6 — Recall Details · AllClear