Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K925126 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Baxter Interlink System Microbore T-Connector Extension Set with 0.22 Micron High Pressure Pediatric... | 1 | 02/06/2003 | Baxter Healthcare Corp. |
Baxter Interlink System Minivolume Extension Set with 0.22 Micron Filter, catalog 1C8577, Baxter Hea... | 1 | 02/06/2003 | Baxter Healthcare Corp. |
Baxter Interlink System Extension Set with 0.22 Micron Filter, catalog 1C8546, Baxter Healthcare Cor... | 1 | 02/06/2003 | Baxter Healthcare Corp. |
Baxter Interlink System Minivolume Extension Set; catalog 1C8483; Baxter Healthcare Corporation, Dee... | 1 | 02/06/2003 | Baxter Healthcare Corp. |
Baxter Interlink System Minivolume Extension Set; catalog 1C8412; Baxter Healthcare Corporation, Dee... | 1 | 02/06/2003 | Baxter Healthcare Corp. |
Y-Type Blood/Solution Set, catalog #1C8372; Standard Blood Filter (170 to 260 micron), Drip Chamber ... | 2 | 01/16/2003 | Baxter Healthcare Corp. |
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