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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2011-2023 - Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60 1 07/17/2023 Olympus Corporation of the Americas
Z-2012-2023 - Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 1 07/17/2023 Olympus Corporation of the Americas
Z-2013-2023 - Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150 1 07/17/2023 Olympus Corporation of the Americas
Z-2017-2023 - Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190 1 07/17/2023 Olympus Corporation of the Americas
Z-2015-2023 - Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170 1 07/17/2023 Olympus Corporation of the Americas
Z-2016-2023 - Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-P180, BF-Q180, BF-Q180-AC, BF-1T180, BF-1TQ180 1 07/17/2023 Olympus Corporation of the Americas
Z-2014-2023 - Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160 1 07/17/2023 Olympus Corporation of the Americas
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