RecallWatchUSA

Home / Recalls / Medical Devices

Aizu Olympus Co., Ltd. recalls Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and en

Recalled November 29, 2023 · FDA recall Z-0346-2024 · Aizu Olympus

Hazard
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 · FDA Class II
Units
0 units
Sold at
Worldwide - US Nationwide distribution.

Description

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

Product
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.
Manufacturer(s)
Aizu Olympus Co., Ltd.
Made in
Japan

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Aizu Olympus Co., Ltd. recalls Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and en | RecallWatchUSA