Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K925126 |
Results per Page |
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 1C8740; An Rx sterile, nonpyrogenic f... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
Baxter Interlink System Y-Type Minivolume Extension Set, product code 1C8645; An Rx sterile, nonpyro... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
Baxter Interlink System Minivolume Extension Set, product code 1C8643; An Rx sterile, nonpyrogenic f... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
Baxter Interlink System Non-DEHP I.V. Catheter Extension Set, 6.6(17 cm), Volume 0.8 mL, Injection ... | 2 | 07/15/2011 | Baxter Healthcare Corp. |
Baxter Interlink System Extension Set, 20" (51 cm), Vol. 2.9 mL, Injection Site, Male Luer Lock Adap... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set, 5.7", Vol. 0.8 mL, 2 Injection Site... | 2 | 05/07/2013 | Baxter Healthcare Corp. |
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