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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| BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 | 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-Q190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Single Use Guide Sheath Kits with the following product descriptions and model numbers: 1... | 1 | 02/11/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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