Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K050220 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number Q180-AC | 1 | 11/09/2023 | Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Model BF-Q180-AC | 2 | 08/31/2023 | Olympus Corporation of the Americas |
| BF-Q180-AC EVIS EXERA II Bronchovideoscope, Model No. BF-Q180-AC | 2 | 09/24/2021 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-Q180-AC | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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