5 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ALLOFT-S ALLOCLASSIC SHL 52/II
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code JDI·March 12, 2019
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 30, 2014
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEN (STANDARD)
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·January 4, 2013
HI-TORQUE PILOT GUIDE WIRE
FDA Adverse Event
Malfunction
·AV-MURRIETA·Product code DQX·November 20, 2010
ALLOFIT-S ALLOCLASSIC, SHELL WITH POLAR SCREW PLUG, UNCEMENTED, 52/II
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 27, 2018