Medical Device Recalls
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11 to 18 of 18 Results
510(K) Number: K061313 |
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 1T180 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| Bronchovideoscope F-1TQ180 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
| Bronchovideoscope BF-Q180 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
| Bronchovideoscope BF-P180 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
| Bronchovideoscope BF-1T180 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-1TQ180: EVIS EXERA II Bronchovideoscope | 2 | 05/06/2022 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-1T180 EVIS EXERA II Bronchovideoscope, Model No. BF-1T180 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
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