Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K842375 |
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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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Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedure... | 2 | 03/05/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
Medtronic DLP, DLP Single Stage Venous Cannula w/Right Angle Metal Tip. Rx Only, Sterile EO, Non... | 2 | 01/18/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
Medtronic, DLP, DLP Right Angle Single Stage Venous Cannulae. Rx Only, Sterile EO, Nonpyrogenic.... | 2 | 01/18/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
Medtronic, Single Stage Venous Cannula, Carmeda Bio-Active Surface Venous Cannula, Sterilized Using ... | 2 | 01/18/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
Medtronic Venous Cannula with bent tip wire, for vascular cardiopulmonary bypass. Catalog Number: ... | 2 | 07/24/2008 | Medtronic Perfusion Systems |
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