Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K964850 |
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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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| Baxter Interlink System Minivolume Extension Set, product code 1C8483; An Rx sterile, nonpyrogenic f... | 2 | 03/24/2006 |
FEI # 1416980 Baxter Healthcare Corp. |
| Baxter Interlink System Minivolume Extension Set, product code 1C8462; 16'', 4.2 mL Vol., with 0.22 ... | 2 | 08/06/2005 |
FEI # 1416980 Baxter Healthcare Corp. |
| Continu-Flo Solution Set, 10 drops/mL, 104'', 0.22 Micron Downstream High Pressure Extended Life Fil... | 2 | 08/21/2003 |
FEI # 1416980 Baxter Healthcare Corp. |
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