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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K133801
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Product Description
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FDA Recall
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Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Pr... 2 05/02/2019 Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX 2 12/27/2024 Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) (GTIN 00085412091570); Mode... 2 03/12/2018 Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX 1 07/17/2025 Baxter Healthcare Corporation
Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library, V8 Spectrum Infusion Pump, Product Co... 2 11/29/2016 Baxter Healthcare Corp.
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