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FDA (Device enforcement)Recalled 2025-05-05class ii

Olympus Corporation of the Americas: Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V

Hazard

Recent post-market surveillance data suggests a possible association of higher microbial contamination levels from TJF duodenoscopes when manual cleaning was delayed beyond one hour and a presoak was performed, compared to those TJF duodenoscopes where manual cleaning began within one hour after patient procedure.

Details from the source

Reason for recall: Recent post-market surveillance data suggests a possible association of higher microbial contamination levels from TJF duodenoscopes when manual cleaning was delayed beyond one hour and a presoak was performed, compared to those TJF duodenoscopes where manual cleaning began within one hour after patient procedure. Distribution: Worldwide Distribution: US (Nationwide) and OUS (International) countries to: Algeria, Angola, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Belarus, Belgium, Benin, Bolivia, Brazil, Canada, Cayman Islands, Chile, Colombia, Costa Rica, Croatia, Denmark, Dominican Republic, Egypt, El Salvador, Estonia, Ethiopia, Faroe Islands, Finland, France, French Guiana, Georgia, Germany, Ghana, Quantity: 12,195 units Lot/code info: UDI-DI: 04953170405563. Model Number: TJF-Q190V. All serial numbers.

UPC codes

04953170405563

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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