10 results
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38ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·November 15, 2020
BD SYRINGE¿ WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·January 12, 2023
SYRINGE S2 2ML 23GA 1-1/4IN BD CHINA
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·January 15, 2021
SYRINGE S2 2ML 23GA 1-1/4IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·November 4, 2019
BD SYRINGE SYRINGE INJECTOR WITHOUT RUBBER STOPPER
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·January 20, 2023
UNIFY CRT-D
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 30, 2014
SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 8, 2013
SIMPLEX P - US TOBRA FD 10-PK
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·November 10, 2010
BD SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·October 1, 2019
BASE SYSTEM ILLU
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM·Product code DXT·March 4, 2024