Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K053512 |
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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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| HomeChoice PRO Automated Peritoneal Dialysis Systems; Catalog Numbers; 5C8310, 5C8310R, R5C8320, R5C... | 1 | 03/01/2010 |
FEI # 3000210122 Baxter Healthcare Renal Div |
| Baxter HomeChoice Automated Peritoneal Dialysis Systems; Catalog Numbers: 5C4471, 5C4471R, 5C4474, ... | 1 | 03/01/2010 |
FEI # 3000210122 Baxter Healthcare Renal Div |
| APD Disposable Sets and Extension Sets used with Baxter HomeChoice and HomeChoice PRO Automated Peri... | 2 | 05/03/2011 |
FEI # 3000210122 Baxter Healthcare Renal Div |
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