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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls Recall Date to: 03/06/2015
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Product Description
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FDA Recall
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Z-0632-2007 - Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2M8063, 2M8063R (refurbished); Baxter Healthcare Corporation, Deerfield, IL 60015 2 03/20/2007 Baxter Healthcare Corp.
Z-0635-2007 - Baxter Flo-Gard 6300 Dual Channel Volumetric Infusion Pump, catalog #2M8048, 2M8048R (refurbished); Baxter Healthcare Corporation, Deerfield, IL 60015 2 03/20/2007 Baxter Healthcare Corp.
Z-0634-2007 - Baxter Flo-Gard 6200 Volumetric Infusion Pump, catalog #2M8043, 2M8043R (refurbished); Baxter Healthcare Corporation, Deerfield, IL 60015 2 03/20/2007 Baxter Healthcare Corp.
Z-0633-2007 - Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump, catalog #2M8064, 2M8064R (refurbished); Baxter Healthcare Corporation, Deerfield, IL 60015 2 03/20/2007 Baxter Healthcare Corp.
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