Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 10/04/2015 510(K) Number: K960280 |
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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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SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to admi... | 2 | 02/04/2015 | CareFusion 303, Inc. |
SmartSite Extension Set, Model No. 20029E, intravascular administration set. | 2 | 04/16/2014 | CareFusion 303, Inc. |
SmartSite Needleless Connector, Model No. 2000E The SmartSite Needleless Connectors are sterile,... | 2 | 02/03/2014 | CareFusion 303, Inc. |
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