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Name Date Date initiated Country Source
Recall of Device Recall Beckman Coulter 2003-08-26 United States USFDA
Recall of Device Recall Cronex 2006-02-16 United States USFDA
Recall of Device Recall Curix 2006-02-16 United States USFDA
Recall of Device Recall Radiomat 2006-02-16 United States USFDA
Recall of Device Recall Brilliance 16 Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Precision Blood Glucose Test Strips 2002-11-08 United States USFDA
Recall of Device Recall Optima 2002-11-26 United States USFDA
Recall of iVIEW DAB Detecion Kit. || Catalog Number 760-091 2003-05-07 United States USFDA
Recall of Device Recall MagNA Pure LC 2003-05-27 United States USFDA
Recall of Device Recall Neonatal Total Galactose Test Kit 2003-05-30 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Neonatal Total Galactose Test Kit 2003-05-30 United States USFDA
Recall of IMMAGE IgM Reagent || Part No.: 447610 2003-06-06 United States USFDA
Recall of Array Systems Calibrator 5 || Part No. 465250 2003-12-17 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of LDL Cholesterol Reagent (LDLD) || Part No. 969706 2003-02-10 United States USFDA
Recall of Device Recall CryoValve 2004-12-17 United States USFDA
Recall of Device Recall Brilliance CT 16 Power Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Ingenuity Core Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Bac T/ALERT 3D Control Module 2005-05-27 United States USFDA
Recall of Device Recall Bac T/ALERT 3D Combination Module 2005-05-27 United States USFDA
Recall of Device Recall Ingenuity Core 128 Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA