Medical Device Recalls
-
1 to 10 of 35 Results
510(K) Number: K023984 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BF-1T60 OES Bronchofiberscope, Model No. BF-1T60 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-3C160: EVIS EXERA Bronchovideoscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-3C40 OES Bronchofiberscope, Model No. BF-3C40 | 2 | 09/24/2021 | 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-XP60 OES Bronchofiberscope, Model No. BF-XP60 | 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 |
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150, BF-1T60, BF-P150 BF-P60 and EVIS EXERA BR... | 1 | 11/09/2023 | Olympus Corporation of the Americas |
Bronchofibercope BF-6C240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
-