medical Class II Updated 2022-06-22

Olympus Corporation of the Americas recalls Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R

Recalled Product

Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R

Hazard / Issue

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.

Issued by

FDA

Affected States: CA, FL, MA, MD, MI, NJ, OH, WI
Lot/Code Info: UDI-DI: 04953170340833 Serial Number: 2836209F 2835978 2837272 2836299
View official government recall

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