Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K230022 |
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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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| Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 | 1 | 07/17/2025 | Baxter Healthcare Corporation |
| Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2 | 2 | 12/27/2024 | Baxter Healthcare Corporation |
| Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the follow... | 2 | 08/16/2024 | Baxter Healthcare Corporation |
| Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2 | 2 | 08/07/2024 | Baxter Healthcare Corporation |
| SIGMA Spectrum Infusion Pump, Product Code 35700BAX2 | 1 | 07/13/2023 | Baxter Healthcare Corporation |
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