4 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BATTERY 14.8V, 6.3 AH LI-ION BATTERY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 5, 2013
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Death
·PHILIPS HEALTHCARE·Product code MKJ·February 3, 2011
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·July 23, 2014
MENTOR MEMORYGEL XTRA BREAST IMPLANT
FDA Adverse Event
Malfunction
·MENTOR TEXAS·Product code FTR·February 26, 2025