Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K211122 |
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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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| Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump | 1 | 08/29/2025 | Baxter Healthcare Corporation |
| Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS | 1 | 08/14/2025 | Baxter Healthcare Corporation |
| Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS | 1 | 05/20/2025 | Baxter Healthcare Corporation |
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