Medical Device Recalls
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21 to 30 of 408 Results
Recall Date from: 08%2F01%2F2018 Recall Date to: 10%2F01%2F2018 Firm: olympus |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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B7-2Q BALLOON CATHETER 13MM DIA 3.2, model no. B7-2Q -Product Usage: Used with endoscopes for inject... | 2 | 02/05/2021 | Aomori Olympus Co., Ltd. |
BF-1T180 EVIS EXERA II Bronchovideoscope, Model No. BF-1T180 | 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-1TQ180: EVIS EXERA II Bronchovideoscope | 2 | 05/06/2022 | 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-MP160F: EVIS EXERA Bronchofibervideoscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-MP60: OES Bronchofiberscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-N20 OES Bronchofiberscope, Model No. BF-N20 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180 | 2 | 09/24/2021 | Olympus Corporation of the Americas |
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