Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K845045 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic, Single Stage Venous Cannula, Carmeda Bio-Active Surface Venous Cannula, Sterilized Using ... | 2 | 01/18/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
| Medtronic DLP, DLP Single Stage Venous Cannulae. Rx Only, Sterile EO, Nonpyrogenic. Model #'s ... | 2 | 01/18/2012 | Medtronic Inc. Cardiac Rhythm Disease Management |
| Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036. | 2 | 09/29/2004 | Medtronic Inc |
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