Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K201758 |
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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 III Bronchovideoscope | 2 | 08/19/2022 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| Olympus Bronchovideoscope, Models BF-P190 & BF-XP190. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190 | 1 | 11/09/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Model No. BF-XP190, EVIS EXERA III Bronchovideoscope | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
| Model No. BF-P190, EVIS EXERA III Bronchovideoscope | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
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