Medical Device Recalls
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61 to 70 of 160 Results
Product Code: eoq |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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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 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number Q180-AC | 1 | 11/09/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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