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U.S. Department of Health and Human Services

Medical Device Recalls
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141 to 150 of 397 Results
Recall Date from: 09%2F29%2F2018 Recall Date to: 09%2F29%2F2018 Firm: Olympus
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BF-MP160F: EVIS EXERA Bronchofibervideoscope 2 05/06/2022 Olympus Corporation of the Americas
BF-1TQ180: EVIS EXERA II Bronchovideoscope 2 05/06/2022 Olympus Corporation of the Americas
BF-MP60: OES Bronchofiberscope 2 05/06/2022 Olympus Corporation of the Americas
Ultrasonic Gastrovideoscope, GF-UC140P-AL5. Intended for endoscopic real-time ultrasound imaging. 2 05/05/2022 Olympus Corporation of the Americas
OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Ol... 2 02/11/2022 Olympus Corporation of the Americas
Spiration Valve System (SVS) Valve in Cartridge -A one-way endobronchial valves indicated for adult ... 2 02/01/2022 Olympus Corporation of the Americas
EVIS EXERA II DUODENOVIDEOSCOPE OLYMPUS TJF-Q180V Model Number: TJF-Q180V 2 12/10/2021 Olympus Corporation of the Americas
ASC PneumoLiner device, Part No. WA90500US (US market only) The Pneumoliner device is intended fo... 2 10/26/2021 Olympus Corporation of the Americas
BF-P60 OES Bronchofiberscope, Model No. BF-P60 2 09/24/2021 Olympus Corporation of the Americas
BF-Q180-AC EVIS EXERA II Bronchovideoscope, Model No. BF-Q180-AC 2 09/24/2021 Olympus Corporation of the Americas
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