ClearanceBrief
Recall Z-0348-2024 ยท FGB Ureteroscope And Accessories, Flexible/Rigid

Aizu Olympus Co., Ltd.

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.

DateNov 17, 2023 (initiated Sep 25, 2023)
StatusOpen, Classified
ReasonChannel 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
Root causeUnder Investigation by firm
ActionOlympus America issued Urgent Medical Device Correction letter on Sept. 25, 2023 to Endoscopy, Respiratory, Pulmonary and Urology Departments, Risk Management Department. Letter states reason for recall, health risk and action to take: Our records indicate that Olympus has serviced your flexible endoscope at one of our Olympus repair facilities. Following repair activities, Olympus uses a water flush of endoscope channels as part of our final endoscope channel inspection, and we subsequently dry the endoscope channels with compressed filtered air. Olympus discovered that our channel air drying
DistributionWorldwide - US Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K172246OLYMPUS URF-V2/V2R
Olympus Medical Systems Corp., Mar 30, 2018
K181451URETERO-RENO VIDEOSCOPE OLYMPUS URF-V3/V3R, URETERO-RENO FIBERSCOPE OLYMPUS URF-P7/P7R
Olympus Medical Systems Corp., Jan 16, 2019