137 results
·
81ms
·
Sources: EU EUDAMED, US FDA
MERSILENE TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code KDC·November 20, 2018
NAIL,FIXATION,BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDS·July 19, 2016
SCREW,FIXATION,BONE
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·July 19, 2016
APPLIANCE,FIXATION,NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·April 26, 2017
SILK SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAP·July 18, 2018
APPLIANCE,FIXATION,NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·April 26, 2016
TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·November 6, 2018
APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·April 26, 2016
TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 5, 2018
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Death
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 24, 2021
PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·September 21, 2018
LEVEEN¿ COACCESS¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code GEI·August 31, 2017
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Death
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 24, 2021
PLATE, FIXATION BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·February 9, 2015
PLATE, FIXATION BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·February 9, 2015
SCREW, FIXATION ,BONE
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·February 9, 2015
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·September 3, 2025
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·September 3, 2025
KINETRA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 7, 2011
UNKNOWN DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·May 18, 2011