Medtronic Bio-Console 560 recall in Canada: manufacturing defect
This recall involves the Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console sold in Canada. It's being recal...
All product recalls associated with Medtronic in Canada, sourced from Health Canada, Transport Canada, and the CFIA.
This recall involves the Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console sold in Canada. It's being recal...
This recall involves the Medtronic HeartWare Ventricular Assist Device (HVAD™) System sold in Canada. It's being recalle...
This recall involves several models of Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchroniz...
This recall involves the Medtronic Carelink Programmer System and related implanted cardiac devices sold in Canada. It's...
This recall involves Medtronic Paradigm Insulin Infusion Pumps (models MMT-508, 522, 722, 554, 754, and others) sold in
This recall involves Medtronic Astra, Azure, Percepta, Serena, and Solara pacemakers and cardiac resynchronization thera...
This recall involves Medtronic Stent Graft Systems sold in Canada. They are being recalled because the sterile barrier m...
This recall involves Medtronic CareLink and Encore Programmers sold in Canada. They are being recalled because a softwar...
This recall involves the Medtronic Adapta, Sensia, and Attesta Pacing Systems sold in Canada. They are being recalled be...
This recall involves Medtronic's EnTrust Dual Chamber Implantable Cardioverter Defibrillators (ICDs) sold in Canada. The...