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Name Date Date initiated Country Source
Recall of Device Recall Engage TR Introducer, 6 F ACT (2.25 mm), 12 cm length, .025" 2010-06-28 United States USFDA
Recall of Device Recall Engage TR Introducer, 6 F ACT (2.25 mm), 25 cm length, .035" 2010-06-28 United States USFDA
Recall of Device Recall Engage TR Introducer, 6 F ACT (2.25 mm), 12 cm length, .035" 2010-06-28 United States USFDA
Recall of Device Recall Engage TR Introducer,6 F ACT (2.25 mm), 12 cm length, .038" 2010-06-28 United States USFDA
Recall of Device Recall Eon Mini Neurostimulation Sysem 2011-05-24 United States USFDA
Recall of Device Recall Rapid Programmer 2009-06-02 United States USFDA
Recall of Device Recall MitraXs" Self Adjusting Atrial Retractor 2011-01-26 United States USFDA
Recall of Neuromodulation systems 2017-09-12 United States USFDA
Recall of Device Recall SJM Confirm, Implantable Cardiac Monitor (ICM) 2011-03-31 United States USFDA
Recall of Accent DR 2011-09-23 United States USFDA
Recall of Anthem CRTP 2011-09-23 United States USFDA
Recall of Eon Mini 3788 (IPG) 2012-09-04 United States USFDA
Recall of Safire Duo Ablation Catheter MediGuide Enabled 2013-10-11 United States USFDA
Recall of US Safire Duo Ablation Catheter MediGuide Enabledand Cool Path Duo Ablation Catheter, MediGuide Enab 2013-10-11 United States USFDA
Recall of FastCath Trio" Hemostasis Introducer 2014-10-14 United States USFDA
Recall of Response Fixed Curve DECA 6F 65cm CSL 2/8 Catheter 2014-10-14 United States USFDA
Recall of Fortify, Unify, Assura, incluging Quadra 2016-10-10 United States USFDA
Recall of Fortify, Unify, Assura, including Quadra 2016-10-10 United States USFDA
Recall of Fortify, Unify, Assura, including Quadra 2016-10-10 United States USFDA
Recall of Neuromodulation systems 2017-09-12 United States USFDA
Recall of Neuromodulation systems 2017-09-12 United States USFDA
Recall of Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 Fr, 15 cm length Obturator supplied as a 10-pack box with 10 Individually packaged Obturators. Sterile EO. Single use. St. Jude medical, DAIG Division, Inc., Minnetonka, MN 55345-2126 USA 2005-09-20 United States USFDA
Recall of Photo DR, Model V-230HV || Implantable Cardioverter Defibrillator 2005-10-06 United States USFDA
Recall of Photo Micro VR/DR Models V-194 2005-10-06 United States USFDA
Recall of Photo Micro VR/DR Models V-232 2005-10-06 United States USFDA