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Medtronic Inc. Cardiac Rhythm Disease Management Recalls

15 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Medtronic Inc. Cardiac Rhythm Disease Management.

15Total Recalls
0Critical
172,093Units Affected
Mar 23, 2015Most Recent
All Recalls

Every Medtronic Inc. Cardiac Rhythm Disease Management Recall

Sorted by most recent. Click any recall for full details.

15 recalls
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT61...
Medical Devices·8,269 affected·Mar 23, 2015
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a cardiac paci...
Medical Implants·6,040 affected·Mar 17, 2015
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Temporary Pacemaker, Model 5348. Single Chamber External Pulse Generator (EPG) Temporary Pacemaker (AAI/VVI). Used in conju...
Cardiac Devices·16,337 affected·Apr 29, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Select CAP Arterial Cannulae. Non-Vented, Carmeda Coated, model CB78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrog...
Medical Devices·19,483 affected·Jan 30, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) an...
Medical Devices·19,483 affected·Jan 30, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Select 3D Arterial Cannulae. Vented, model 78624 (24 Fr.). Non-Vented Cannulae, model 78724 (24 Fr.). Sterilized using Ethy...
Medical Devices·19,483 affected·Jan 30, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Cannulae. Model 3Y90R3, the following model is onl...
Medical Devices·19,483 affected·Jan 30, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 78722 (22 Fr.). Sterilized using Ethy...
Medical Devices·19,483 affected·Jan 30, 2014
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model Numbers: CB1D82R12 and CB5N73R7. Sterilized by Ethylene Oxid...
Medical Devices·217 affected·Jul 17, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Custom Perfusion System. Model Numbers: 1D80R8, 1E34R1, 1F75R1, 1G49R2, 1G75R1, 1P07R8, 1P91R4, 5B15R11, and 5P51R9. Steri...
Medical Devices·13,223 affected·Jul 17, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Custom Perfusion System with Trillium BioSurface (a polymer containing non-leaching heparin). Model Numbers: TL4X17R8, TL5D01...
Medical Devices·758 affected·Jul 17, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic, Launcher Guiding Catheter, Model # LA8EBU45SH, Lot # 0006722866, 8F and Model # LA6IMAD, Lot # 0006724224, 6F Product Usa...
Surgical Devices·15 affected·Jun 12, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic, Consulta¿ CRT-P, Model C4TR01, C3TR01 (not approved for US), and Syncra¿ CRT-P, Model C2TR01, Sterile EO. Dual chamber ...
Medical Devices·1,912 affected·Jun 7, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm), Model ARCSJ200W. Intended to facilitate catheter placement and exchange du...
Surgical Devices·225 affected·Mar 13, 2013
High RiskFDA
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Models ARCSJ200W, ARCSJ260W, and ARCDJ260W. Sterile using ethylene oxide. ...
Surgical Devices·27,682 affected·Mar 13, 2013