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Name Date Date initiated Country Source
Recall of Telesheath Catheter TwoPiece Introducer Kit with Hemostasis Valve 2004-08-04 United States USFDA
Recall of Telesheath Catheter TwoPiece Introducer Kit with Hemostasis Valve 2004-08-04 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 Micro VR/DR Models V-232 2005-10-06 United States USFDA
Recall of Atlas VR, Models V-199 2005-10-06 United States USFDA
Recall of Photo DR, Model V-230HV || Implantable Cardioverter Defibrillator 2005-10-06 United States USFDA
Recall of Atlas DR, Models V-240 2005-10-06 United States USFDA
Recall of Photo Micro VR/DR Models V-194 2005-10-06 United States USFDA
Recall of Device Recall AngioSeal 2006-06-07 United States USFDA
Recall of Identity 2006-10-06 United States USFDA
Recall of Merlin PCS Programmer 2006-10-06 United States USFDA
Recall of APS III 2006-10-06 United States USFDA
Recall of Device Recall St Jude Medica CPS Direct SL 2007-03-20 United States USFDA
Recall of Device Recall Epic VR Model V197 2008-01-16 United States USFDA
Recall of Device Recall Epic HF Model V338 2008-01-16 United States USFDA
Recall of Device Recall Epic DR Model V235 2008-01-16 United States USFDA
Recall of Device Recall Epic HF Model V339 2008-01-16 United States USFDA
Recall of Device Recall Epic DR Model V239 2008-01-16 United States USFDA
Recall of Device Recall ATLAS DR Model V242 2008-01-16 United States USFDA
Recall of Device Recall Epic II HF Model V355 2008-01-16 United States USFDA
Recall of Device Recall Epic II VR Model V158 2008-01-16 United States USFDA
Recall of Device Recall Epic II HF Model V357 2008-01-16 United States USFDA
Recall of Device Recall Epic VR Model V196 2008-01-16 United States USFDA
Recall of Device Recall Epic HF Model V337 2008-01-16 United States USFDA
Recall of Device Recall Epic II DR Model V255 2008-01-16 United States USFDA