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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 41 Results
510(K) Number: K023984
 
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Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60 1 07/17/2023 FEI # 2429304
Olympus Corporation of the Americas
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160 1 07/17/2023 FEI # 2429304
Olympus Corporation of the Americas
Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT... 2 08/31/2023 FEI # 2429304
Olympus Corporation of the Americas
Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150 1 07/17/2023 FEI # 2429304
Olympus Corporation of the Americas
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 1 07/17/2023 FEI # 2429304
Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 1 10/16/2025 FEI # 2429304
Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 1 10/16/2025 FEI # 2429304
Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 1 10/16/2025 FEI # 2429304
Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 1 10/16/2025 FEI # 2429304
Olympus Corporation of the Americas
EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 1 10/16/2025 FEI # 2429304
Olympus Corporation of the Americas
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