8 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 6, 2025
BD 10ML SYRINGE * SERINGUE LUER-LOK TIP, EMBOUTBD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·April 7, 2025
ECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code BSP·November 21, 2019
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·March 22, 2013
CURITY 3.0MM CUFFED
FDA Adverse Event
Injury
·COVIDIEN / FORMERLY TYCO HEALTHCARE·Product code BTR·March 18, 2011
MAVERICK2 MONORAIL PTCA CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·April 16, 2008
ECHOTIP ULTRA CELIAC PLEXUS NEUROLYSIS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·July 5, 2023
3 ML BD LUER-LOK¿ SYRINGE WITH ATTACHED BD¿ BLUNT FILL NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 9, 2021