Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K250862 |
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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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| BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 | 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 |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 | 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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