1,067 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
*
FDA Adverse Event
Death
·HBR·Product code FNL·September 8, 1999
HBR HEALTHCARE CO
FDA Adverse Event
Injury
·HILL-ROM·Product code FNL·October 15, 1992
XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code NIQ·August 21, 2025
SYNERGY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 7, 2025
XIENCE EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Death
·ABBOTT VASCULAR·Product code NIQ·August 21, 2025
SYNERGY
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 7, 2025
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
ACTIVE® INHIBIN A ELISA, 4X96 WELLS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code NDR·June 1, 2011
TANDEM CEA ERA
FDA Adverse Event
Malfunction
·HIBRITECH, INC.·Product code DHX·November 14, 1996
UNK
FDA Adverse Event
Death
·HBR HEALTHCARE CO·Product code FNJ·April 20, 1998
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code MMI·June 2, 2021
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code MMI·October 13, 2020
ARCHITECT CA 125 II
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LTK·July 10, 2012
ARCHITECT CA 125 II
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LTK·July 9, 2012