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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K041191
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 2 01/11/2007 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 2 01/11/2007 Baxter Healthcare Corp.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 01/31/2006 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 01/31/2006 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 09/23/2005 Baxter Healthcare Corp.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 09/23/2005 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 07/21/2005 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 07/21/2005 Baxter Healthcare Corp.
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