Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K190910 |
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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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| Hemodialysis Delivery System, Software Version 2.x. | 2 | 11/11/2021 |
FEI # 1417572 Baxter Healthcare Corporation |
| PrisMax V2-US, Hemodialysis Delivery System, Product Codes: 955626, 955558, 955627, 955701 | 2 | 08/26/2025 |
FEI # 3038195011 VANTIVE US HEALTHCARE LLC |
| The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Asse... | 2 | 02/26/2021 |
FEI # 1417572 Baxter Healthcare Corporation |
| TherMax Blood Warmer Unit | 2 | 10/30/2019 |
FEI # 1417572 Baxter Healthcare Corporation |
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