Medical Device Recalls
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61 to 70 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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|---|---|---|---|
| Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-XT190. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-MP190F. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-1TH190, BF-H190, BF-Q170, & BF-Q190. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Airway Mobilescope, Models MAF-GM & MAF-TM. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-1T180, BF-1TQ180, BF-P180, & BF-Q180. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Model BF-Q180-AC | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-MP160F, BF-XP160F, BF-XP60. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT... | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
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