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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls Recall Date to: 07/31/2014
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Z-0995-2014 - Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) and 78720 (20 Fr.). Sterilized using Ethylene Oxide. Non-pyroge... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
Z-0996-2014 - Medtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Cannula consists of a curv... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
Z-1000-2014 - Medtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Cannulae. Model 3Y90R3, the following model is only approved in Europe C300901B. Sterilized using Ethylene Oxide... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
Z-0998-2014 - Medtronic Select CAP Arterial Cannulae. Vented, models 78818 (18 Fr.), 78820 (20 Fr.), 78822 (22 Fr.). Non-Vented Cannulae, model 78920 (20 Fr.), 78922 (22 Fr.), 78924 (24 Fr.). Sterilized using E... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
Z-0999-2014 - Medtronic Select CAP Arterial Cannulae. Non-Vented, Carmeda Coated, model CB78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Select 3D Arterial Cannulae has clear flexible, ... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
Z-0997-2014 - Medtronic Select 3D Arterial Cannulae. Vented, model 78624 (24 Fr.). Non-Vented Cannulae, model 78724 (24 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Cannula consists of a curv... 2 02/20/2014 Medtronic Inc. Cardiac Rhythm Disease Management
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