Medtronic Inc. Cardiac Rhythm Disease Management: 18 recalls on record

Recalls filed with 1 agency: FDA (18).

First recall on record: January 9, 2013. Most recent: June 4, 2014.

Risk classification: Class II: 18

Most recent recalls

DateAgencyProduct
June 4, 2014FDAMedtronic Temporary Pacemaker, Model 5348. Single Chamber External Pulse Generator (EPG) …Z-1661-2014
February 26, 2014FDAMedtronic Select CAP Arterial Cannulae. Non-Vented, Carmeda Coated, model CB78722 (22 Fr…Z-0999-2014
February 26, 2014FDAMedtronic Select CAP Arterial Cannulae. Vented, models 78818 (18 Fr.), 78820 (20 Fr.), …Z-0998-2014
February 26, 2014FDAMedtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Can…Z-1000-2014
February 26, 2014FDAMedtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.)…Z-0995-2014
February 26, 2014FDAMedtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannul…Z-0996-2014
February 26, 2014FDAMedtronic Select 3D Arterial Cannulae. Vented, model 78624 (24 Fr.). Non-Vented Cannul…Z-0997-2014
September 4, 2013FDAMedtronic Custom Perfusion System. Model Numbers: 1D80R8, 1E34R1, 1F75R1, 1G49R2, 1G75R…Z-2104-2013
September 4, 2013FDAMedtronic Custom Perfusion System with Carmeda BioActive Surface. Model Numbers: CB1D82…Z-2105-2013
September 4, 2013FDAMedtronic Custom Perfusion System with Trillium BioSurface (a polymer containing non-leac…Z-2106-2013
August 21, 2013FDAMedtronic Affinity Pediatric Arterial Filter, model number S4014, sterilized using ethyle…Z-1966-2013
August 14, 2013FDAMedtronic Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of …Z-1876-2013
July 3, 2013FDAMedtronic, Launcher Guiding Catheter, Model # LA8EBU45SH, Lot # 0006722866, 8F and Model…Z-1564-2013
July 3, 2013FDAMedtronic, Consulta¿ CRT-P, Model C4TR01, C3TR01 (not approved for US), and Syncra¿ CRT…Z-1607-2013
April 3, 2013FDAMedtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm), Model ARCSJ200W. Intended …Z-1017-2013
April 3, 2013FDAMedtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Models ARCSJ200W, ARCSJ260W,…Z-1019-2013
March 13, 2013FDAMedtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypas…Z-0908-2013
January 9, 2013FDAMedtronic Intersept Custom Tubing Pack with or without coating ( Carmeda BioActive Surfac…Z-0618-2013

Questions about this company

How many recalls does Medtronic Inc. Cardiac Rhythm Disease Management have?
Recalert has 18 U.S. recalls on record for Medtronic Inc. Cardiac Rhythm Disease Management, published between January 9, 2013 and June 4, 2014.
What was the most recent Medtronic Inc. Cardiac Rhythm Disease Management recall?
FDA recall Z-1661-2014, published June 4, 2014: Medtronic Temporary Pacemaker, Model 5348. Single Chamber External Pulse Generator (EPG) Temporary Pacemaker (AAI/VVI). Used in conjunction with a cardiac pacing lead system for temporary atrial …
Which agencies have handled Medtronic Inc. Cardiac Rhythm Disease Management recalls?
Medtronic Inc. Cardiac Rhythm Disease Management appears as the recalling firm in recalls from: FDA (18).

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