8 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VENFLON I 20GA 1.0 MM X 32MM
FDA Adverse Event
Malfunction
·Product code FOZ·August 24, 2021
COBAS EGFR MUTATION TEST
FDA Adverse Event
ROCHE MOLECULAR SYSTEMS, INC.·Product code OWD·January 29, 2014
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 8, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 20, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·August 14, 2008
PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 18, 2013
PROMUS ELEMENT¿ PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 18, 2012
COBAS EGFR MUTATION TEST
FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code OWD·January 14, 2015