Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K230041 |
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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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| Spectrum IQ Infusion Pump, Product Code 3570009 | 2 | 08/22/2025 | Baxter Healthcare Corporation |
| Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 | 1 | 03/06/2025 | Baxter Healthcare Corporation |
| Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 | 2 | 11/08/2024 | Baxter Healthcare Corporation |
| Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 357... | 2 | 08/16/2024 | Baxter Healthcare Corporation |
| Spectrum IQ Infusion pump, Product Code 357009 | 2 | 05/13/2024 | Baxter Healthcare Corporation |
| Baxter Spectrum IQ Infusion Pump, Product Code 3570009 | 2 | 05/03/2024 | Baxter Healthcare Corporation |
| The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009 | 1 | 07/13/2023 | Baxter Healthcare Corporation |
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