Medical Device Recalls
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11 to 20 of 160 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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|---|---|---|---|
| BF-MP60: OES Bronchofiberscope | 2 | 05/06/2022 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-N20 OES Bronchofiberscope, Model No. BF-N20 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-P60 OES Bronchofiberscope, Model No. BF-P60 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-Q180-AC EVIS EXERA II Bronchovideoscope, Model No. BF-Q180-AC | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-XP160F EVIS EXERA Bronchovideoscope, Model No. BF-XP160F | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-XT160 EVIS EXERA Bronchovideoscope, Model No. BF-XT160 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 | 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 |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
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