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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 Cordis S.M.A.R.T. Flex Vascular Stent System 2017-02-16 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 Device Recall CryoValve 2004-03-24 United States USFDA
Recall of Device Recall AMPLICOR HPV Master Mix Analyte Specific Reagent 2004-03-10 United States USFDA
Recall of Device Recall AMPLICOR HPV Microwell Plate Analyte Specific Reagent 2004-03-10 United States USFDA
Recall of Device Recall Precision Blood Glucose Test Strips 2002-11-08 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 Device Recall Optima 2002-11-26 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 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 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 Device Recall Neonatal Total Galactose Test Kit 2003-05-30 United States USFDA
Recall of Device Recall Brilliance BigBore Oncology Computed Tomography Xray systems, 2016-03-24 United States USFDA
Recall of Device Recall Brilliance BigBore Radiology Computed Tomography Xray systems 2016-03-24 United States USFDA
Recall of Digital Radiography System, model DFP-8000D 2004-06-18 United States USFDA
Recall of Device Recall CryoValve 2004-12-17 United States USFDA