3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CHLORAPREP ONE-STEP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code KXF·August 20, 2020
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·January 24, 2022
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 1, 2011