3 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·July 8, 2014
SYRINGE S2 2ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·December 23, 2020