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Name Date Date initiated Country Source
Recall of Device Recall Elecsys 2006-01-31 United States USFDA
Recall of Device Recall CryoValve 2006-01-27 United States USFDA
Recall of Device Recall CEDIA 2006-02-10 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall Fem IM Nail 15mmdx48cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Fem IM Nail 16mmdx48cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Natus neoBLUE 2 Phototherapy system 2014-11-19 United States USFDA
Recall of Device Recall Nuclear, Magnetic Resonance Imaging 2018-03-16 United States USFDA
Recall of Device Recall INSTRUMENT ARM DRAPE, IS4000, 20 PACK 2015-06-16 United States USFDA
Recall of Device Recall OSSEOTITE Certain 2 Implant 2014-11-07 United States USFDA
Recall of Device Recall SOMATOM Spirit(Model 10045692 ) 2018-02-01 United States USFDA
Recall of Device Recall D240 (Lymphatic Marker) 2015-05-06 United States USFDA
Recall of Device Recall Cios Alpha 2015-05-05 United States USFDA
Recall of Device Recall BrainLAB Image Guided Surgery (IGS) System VectorVision fluoro 3D 2015-05-08 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Smiths Medical 2014-11-21 United States USFDA
Recall of Device Recall Max Implant 2015-01-23 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall Fem IM Nail 15mmdx50cm, Sterile, 2017-02-28 United States USFDA
Recall of Device Recall Intravascular Ultrasound System 2015-06-22 United States USFDA
Recall of Device Recall STAIA PACK IRIInsulin 2018-03-05 United States USFDA
Recall of Device Recall 100/120V AC, Advanced Perfusion System Platform (APS) 2015-05-01 United States USFDA
Recall of Device Recall Brilliance CT Big Bore Oncology 2015-03-16 United States USFDA
Recall of Device Recall Brilliance CT 64 2015-03-16 United States USFDA