Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K123733 |
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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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| Cardioblate CryoFlex Surgical Ablation Console | 2 | 11/19/2021 |
FEI # 1000116158 Medtronic Perfusion Systems |
| Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60CM1, CLAMP 60CM1 CRYOFLEX PROBE 26L - ... | 2 | 11/25/2020 |
FEI # 3008592544 MEDTRONIC ATS MEDICAL, INC. |
| Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF2, PROBE 60SF2 CRYOFLEX 10CM 26L - P... | 2 | 11/25/2020 |
FEI # 3008592544 MEDTRONIC ATS MEDICAL, INC. |
| Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF3, PROBE 60SF3 CRYOFLEX 10-S 26L - i... | 2 | 11/25/2020 |
FEI # 3008592544 MEDTRONIC ATS MEDICAL, INC. |
| Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF7, PROBE 60SF7 CRYOFLEX 7CM 26L - is... | 2 | 11/25/2020 |
FEI # 3008592544 MEDTRONIC ATS MEDICAL, INC. |
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