4 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
AUTOPULSE® LI-ION BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC·Product code DRM·April 24, 2014
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 27, 2012
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·July 27, 2010
K-FILE M-ACCESS 25MM 030
FDA Adverse Event
Malfunction
·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKS·December 8, 2025