Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K891687 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Extra corporeal circuit with bio-active surface. | 2 | 07/04/2020 |
FEI # 1000116158 Medtronic Perfusion Systems |
| Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS... | 3 | 02/26/2016 |
FEI # 1000116158 Medtronic Perfusion Systems |
| Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model Numbers: CB1D82R12 and CB5... | 2 | 08/27/2013 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
| Custom Packs/Mexico, Medtronic Cardio-Kit, Sterilized Using Ethylene Oxide, Nonpyrogenic, Rx Onl... | 2 | 01/18/2012 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
| Medtronic Extracorporeal Circuit with bio-active surface; Cardiopulmonary Bypass Oxygenator, Catal... | 2 | 07/24/2008 |
FEI # 1000116158 Medtronic Perfusion Systems |
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