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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K012988
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Product Description
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FDA Recall
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HomeChoice PRO Automated Peritoneal Dialysis Systems; Catalog Numbers; 5C8310, 5C8310R, R5C8320, R5... 2 03/07/2008 Baxter Healthcare Renal Div
Spanish Patient At-Home Guide for the HomeChoice/HomeChoice Pro Automated Peritoneal Dialysis System... 3 11/16/2005 Baxter Healthcare Renal Div
HomeChoice PRO Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation... 2 07/19/2005 Baxter Healthcare Renal Div
HomeChoice PRO Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation... 2 01/15/2005 Baxter Healthcare Renal Div
HomeChoice and Yume Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corpor... 2 11/11/2004 Baxter Healthcare Renal Div
HomeChoice PRO and Yume Plus Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthca... 2 11/11/2004 Baxter Healthcare Renal Div
HomeChoice PRO and Yume PlusAutomated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcar... 2 07/20/2004 Baxter Healthcare Renal Div
HomeChoice PRO Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation... 3 02/21/2003 Baxter Healthcare Corp.
HomeChoice Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation, De... 3 02/21/2003 Baxter Healthcare Corp.
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