11 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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GORE TAG THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 14, 2021
CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 14, 2020
GORE® EXCLUDER®AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·June 27, 2022
TENDRIL SDX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·September 8, 2011
CELL-DYN WBC REAGENT A
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 24, 2008
HOMECHOICE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 22, 2013
CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 3, 2021
GORE TAG CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 23, 2020
ENDO GIA
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·May 24, 2023
SIGNIA
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·May 4, 2023
ENDO GIA ULTRA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·December 18, 2023