5 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ONE TOUCH BASIC ENHANCED METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·July 28, 2009
NIAGARA DIALYSIS CATHETER KIT 13.5 F X 24 CM (SHORT-TERM)
FDA Adverse Event
Malfunction
·C.R. BARD INC. (BASD)·Product code MPB·March 21, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012
1644487-2008-00513
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·February 29, 2008
HANCOCK AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·November 8, 2019