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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 60 of 393 Results
Recall Date from: 09%2F29%2F2018 Recall Date to: 09%2F29%2F2018 Firm: Olympus
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Model No. ENF-XP, RHINO-LARYNGOFIBERSCOPE 2 01/09/2024 Shirakawa Olympus Co., Ltd.
Model No. BF-XP190, EVIS EXERA III Bronchovideoscope 2 01/09/2024 Shirakawa Olympus Co., Ltd.
Model No. CYF-5, Cystonephrofiberscope 2 01/09/2024 Shirakawa Olympus Co., Ltd.
Model No. CYF-5R, Cystonephrofiberscope 2 01/09/2024 Shirakawa Olympus Co., Ltd.
Model No. BF-P190, EVIS EXERA III Bronchovideoscope 2 01/09/2024 Shirakawa Olympus Co., Ltd.
OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a vi... 2 01/05/2024 Olympus Corporation of the Americas
OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model: LTF-S190-10 Used with a vide... 2 01/05/2024 Olympus Corporation of the Americas
ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Rig... 2 12/15/2023 Olympus Corporation of the Americas
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP 2 12/14/2023 Olympus Corporation of the Americas
PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE 2 11/29/2023 Aizu Olympus Co., Ltd.
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