8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VACUTAINER CPT CELL PREPARATION TUBE WITH SODIUM HEPARIN
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·January 8, 2021
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 27, 2009
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·December 16, 2010
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 4, 2013
EXTRACTION SCREWDRIVER
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HXX·March 28, 2011
INSIGNIA ENTRA
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008
EMBOSHIELD NAV6 EMBOLIC PROTECTION SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NTE·June 14, 2012
BD VACUTAINER CPT CELL PREPARATION TUBE WITH SODIUM HEPARIN
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 15, 2020