9 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
EVOLUT R TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 14, 2018
VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·November 16, 2017
OLYMPUS EVIS EXERA II PEDI VIDEO COLONOSCOPE
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDF·June 28, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 5, 2011
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·February 8, 2018
SILK SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAP·November 16, 2017
ETHILON NYLON SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAR·November 16, 2017
UNK_CELSIUS THERMOCOOL
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·February 21, 2019
UNK_SMART TOUCH BIDIRECTIONAL
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code OAD·February 21, 2019