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 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 |
BF-3C160: EVIS EXERA Bronchovideoscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-MP60: OES Bronchofiberscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-P60 OES Bronchofiberscope, Model No. BF-P60 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-1T60 OES Bronchofiberscope, Model No. BF-1T60 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-XP60 OES Bronchofiberscope, Model No. BF-XP60 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-3C40 OES Bronchofiberscope, Model No. BF-3C40 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-XT160 EVIS EXERA Bronchovideoscope, Model No. BF-XT160 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160 | 2 | 09/21/2021 | Olympus Corporation of the Americas |
Bronchofiberscope BF-40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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