6 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BD PLASTIPAK LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 4, 2020
BD PLASTIPAK LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 9, 2020
SINGLE 8 EXTENSION
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010
INGENIO
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014
AFFINITY IV BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code HDD·November 28, 2012
SYRINGE NON STERILE 50ML LL
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·October 20, 2020