medical Class II Updated 2022-06-22

Olympus Corporation of the Americas recalls Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5

Recalled Product

Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5

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: 04953170339417 Serial Number: 2456630 7171632 2769732 W501648A 2355088 2557155 2972060
View official government recall

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