Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K883111 |
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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 1550 Single Patient System Hemodialysis Machines; Baxter Healthcare Corporation, Deerfield, I... | 2 | 04/12/2010 | Baxter Healthcare Renal Div |
Baxter 1550 Single Patient System Hemodialysis Machines; Baxter Healthcare Corporation, Deerfield, I... | 2 | 03/20/2003 | Baxter Healthcare Corp. |
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