Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K923065 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic Container, PL-146 used ... | 2 | 08/02/2012 |
FEI # 3000210122 Baxter Healthcare Renal Div |
| Baxter HomeChoice Automated Peritoneal Dialysis Systems; Catalog Numbers: 5C4471, 5C4471R, 5C4474, 5... | 2 | 03/07/2008 |
FEI # 3000210122 Baxter Healthcare Renal Div |
| HomeChoice Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation, De... | 2 | 07/19/2005 |
FEI # 3000210122 Baxter Healthcare Renal Div |
| HomeChoice and Yume Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corpor... | 2 | 07/20/2004 |
FEI # 3000210122 Baxter Healthcare Renal Div |
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