Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K915523 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump; Baxter Healthcare Corporation, Deerfield... | 2 | 10/28/2011 | Baxter Healthcare Corp. |
Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump; Baxter Healthcare Corporation, Deerfield... | 1 | 07/28/2007 | Baxter Healthcare Corp. |
Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump, catalog #2M8064, 2M8064R (refurbished); ... | 2 | 03/20/2007 | Baxter Healthcare Corp. |
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