Medical Device Recalls
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510(K) Number: K023984 |
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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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| Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Mo... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 | 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 TYPE 1T150 | 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 |
| EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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