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Recall Observatory FDA recall evidence

Device product

Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.

Z-0348-2024

September 25, 2023

Class II

Product summary

Firm
Aizu Olympus Co., Ltd.
Event
Event 93222
Status
Ongoing
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-0348-2024

Official wording

Reason: Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Code information: Model Number (UDI-DI): URF-P7 (04953170403811), URF-P7R (04953170403835), URF-V2 (04953170343582), URF-V2R (04953170343612), URF-V3 (04953170403385), URF-V3R (04953170403392).

Distribution pattern: Worldwide - US Nationwide distribution.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    contamination that could lead