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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K915522
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Product Description
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FDA Recall
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Baxter Flo-Gard 6201, Single Channel Volumetric Infusion Pump; Baxter Healthcare Corporation, Deerfi... 2 04/29/2011 FEI # 1416980
Baxter Healthcare Corp.
Baxter FloGard 6201 Volumetric Infusion Pump. Baxter Healthcare Corporation, Medication Delivery Di... 2 01/21/2011 FEI # 1416980
Baxter Healthcare Corp.
Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2M8063, 2M8063R (refurbished); Baxter Health... 2 03/20/2007 FEI # 1416980
Baxter Healthcare Corp.
Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump, catalog #2M8064, 2M8064R (refurbished), ... 2 09/21/2005 FEI # 1416980
Baxter Healthcare Corp.
Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2M8063, 2M8063R (refurbished), 2M8063G (glob... 2 09/21/2005 FEI # 1416980
Baxter Healthcare Corp.
Baxter Flo-Gard 6201, SIngle Channel , Volumetric Infusion Pump; Baxter Healthcare Corporation, Dee... 1 07/28/2007 FEI # 1416980
Baxter Healthcare Corp.
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