Medical Device Recalls
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21 to 30 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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| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150, BF-1T60, BF-P150 BF-P60 and EVIS EXERA BR... | 1 | 11/09/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 | 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 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 | 1 | 10/16/2025 |
FEI # 2429304 Olympus Corporation of the Americas |
| Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the... | 2 | 11/25/2020 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Descr... | 2 | 11/26/2025 |
FEI # 3021325287 Noah Medical Corporation |
| Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127... | 2 | 01/21/2026 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| Bronchofibercope BF-6C240 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
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