ClearanceBrief
Recall Z-0346-2024 ยท FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

Aizu Olympus Co., Ltd.

Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbers: TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.

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
Quantity0 units
DistributionWorldwide - US Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K143153EVIS EXERA II DUODENOVIDEOSCOPE OLYMPUS TJF TYPE Q180V
Olympus Medical Systems Corp., Jan 15, 2016
K193182Evis Exera III Duodenovideoscope Olympus TJF-Q190V
Olympus Medical Systems Corp., Jan 17, 2020
K954451EVIS 140 SYSTEM
Olympus America, Inc., Mar 29, 1996