1,811 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
SFL LEAD, TRANSVENOUS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 15, 2014
VACUTAINER ++SF-L 25G 3/4
FDA Adverse Event
Injury
·BECTON DICKINSON AND COMPANY·Product code FMI·January 12, 2021
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Injury
·CONCORD MANUFACTURING·Product code FKX·December 19, 2022
DAVINCI XI
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC·Product code NAY·March 25, 2025
TENDRIL STS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. (CRM-KISTA)·Product code NVN·May 24, 2016
PROMUS ELEMENT? PLUS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·September 17, 2014
16G X 1.16IN (1.7 X 30 MM) ANGIOCATH
FDA Adverse Event
Injury
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·October 30, 2019
COMPLETE MOISTURE PLUS
FDA Adverse Event
Injury
·AMERICAN MEDICAL OPTICS·Product code LPN·June 2, 2007
REMEEX SYSTEM FOR URINARY INCONTINENCE
FDA Adverse Event
Injury
·DIMA S.L.·Product code FTL·February 22, 2012
CERAROOT ZIRCONIUM OXIDE DENTAL IMPLANT
FDA Adverse Event
Injury
·CERAROOT S.L.·Product code DZE·May 20, 2021
REMEEX SYSTEM FOR URINARY INCONTINENCE
FDA Adverse Event
Injury
·DIMA S.L.·Product code FTL·June 8, 2012
KLOCKNER DENTAL IMPLANTS
FDA Adverse Event
Injury
·SOADCO, S.L.·Product code DZE·August 19, 2004
KLOCKNER DENTAL IMPLANTS
FDA Adverse Event
Injury
·SOADCO, S.L.·Product code DZE·August 19, 2004
KLOCKNER DENTAL IMPLANTS
FDA Adverse Event
Injury
·SOADCO, S.L.·Product code DZE·August 19, 2004
NEEDLELESS SLING
FDA Adverse Event
Injury
·DIMA S.L.·Product code PAH·June 11, 2020
NEEDLELESS SLING
FDA Adverse Event
Injury
·DIMA S.L.·Product code PAH·June 11, 2020
REMEEX SYSTEM FOR FEMALE URINARY INCONTINENCE
FDA Adverse Event
Injury
·DIMA S.L.·Product code OTN·May 28, 2020
NEEDLELESS SLING
FDA Adverse Event
Injury
·DIMA S.L.·Product code PAH·June 11, 2020
REMEEX SYSTEM
FDA Adverse Event
Injury
·DIMA S.L.·Product code OTN·July 29, 2021
MALE REEMEX SYSTEM
FDA Adverse Event
Injury
·DIMA S.L.·Product code FTL·July 7, 2009