Medical Device Recalls
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1 to 10 of 155 Results
Product Code: eoq |
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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| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| 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 Q180 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 | 1 | 10/16/2025 | Olympus Corporation of the Americas |
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