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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 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 FEI # 1314492
Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), infusion pump, 35700BAX2 ... 2 06/07/2018 FEI # 1314492
Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) (GTIN 00085412091570); Mode... 2 03/12/2018 FEI # 1314492
Baxter Healthcare Corporation
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library, Model #/Product Code 35700BAX2 2 10/02/2017 FEI # 1314492
Baxter Healthcare Corporation
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