Medical Device Recalls
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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 III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 | 1 | 10/16/2025 |
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 |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 | 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 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 | 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 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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