Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K022272 |
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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 Venous Cannulae: a) DLP® 20 Fr. Malleable Single Stage Venous Cannula, Model Number 681... | 2 | 05/10/2024 | Medtronic Perfusion Systems |
Medtronic, DLP, DLP Malleable Single Stage Venous Cannulae. Rx Only, Sterilized Using Ethylene Ox... | 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 |
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