Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K242390 |
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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 Syringe Pump, Product Code 40800BAXUS, infusion pump | 1 | 08/29/2025 | Baxter Healthcare Corporation |
| Baxter Novum IQ Syringe Pump, product code 40800BAXUS, | 2 | 06/12/2025 | Baxter Healthcare Corporation |
| Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS | 2 | 03/21/2025 | Baxter Healthcare Corporation |
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