Medical Device Recalls
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1 to 10 of 35 Results
510(K) Number: K023984 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60 | 1 | 07/17/2023 | Olympus Corporation of the Americas |
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160 | 1 | 07/17/2023 | 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 | Olympus Corporation of the Americas |
Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150 | 1 | 07/17/2023 | Olympus Corporation of the Americas |
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 | 1 | 07/17/2023 | Olympus Corporation of the Americas |
EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160 | 2 | 09/21/2021 | Olympus Corporation of the Americas |
Bronchovidescope BF-1T240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovideoscope BF-XT160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovideoscope BF-XP160F | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovideoscope BF-P240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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