Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K131497 |
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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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| Change Healthcare Cardiology Hemo Software | 2 | 07/02/2025 |
FEI # 3003757840 CHANGE HEALTHCARE CANADA COMPANY |
| McKesson Cardiology Hemo software | 2 | 01/16/2025 |
FEI # 3394 A L I Technologies Ltd |
| Change Healthcare Cardiology Hemo software | 2 | 01/16/2025 |
FEI # 3394 A L I Technologies Ltd |
| Change Healthcare Cardiology Hemo. Versions 14.2, 14.1.1, 14.2, 14.3, 14.3.2, 14.3, 15.0.1, 15.1. ... | 2 | 10/17/2024 |
FEI # 3003757840 CHANGE HEALTHCARE CANADA COMPANY |
| McKesson Cardiology Hemo. Versions 13.0, 13.1.1, 13.1.2, 13.2, 13.2.1, 14.0. | 2 | 10/17/2024 |
FEI # 3003757840 CHANGE HEALTHCARE CANADA COMPANY |
| Horizon Cardiology Hemo | 2 | 05/24/2019 |
FEI # 3007784465 Change Healthcare Israel Ltd. |
| McKesson Cardiology Hemo | 2 | 05/24/2019 |
FEI # 3007784465 Change Healthcare Israel Ltd. |
| McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and dat... | 2 | 08/31/2018 |
FEI # 3007784465 McKesson Israel Ltd. |
| McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemody... | 2 | 10/20/2014 |
FEI # 3002684279 Mckesson Information Solutions LLC |
| McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data ... | 2 | 10/08/2014 |
FEI # 3002684279 Mckesson Information Solutions LLC |
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