Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K133801 |
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 V6, Model Number 35700BAX | 1 | 07/17/2025 | Baxter Healthcare Corporation |
| Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX | 1 | 03/06/2025 | Baxter Healthcare Corporation |
| Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product code 35700BAX2. | 1 | 01/29/2022 | Baxter Healthcare Corporation |
| Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) | 1 | 10/22/2020 | Baxter Healthcare Corporation |
| Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) | 1 | 10/22/2020 | Baxter Healthcare Corporation |
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