114 results
·
103ms
·
Sources: EU EUDAMED, US FDA
TRAPEASE UNKNOWN FILTER
FDA Adverse Event
Injury
·CORDIS RODEN·Product code DTK·March 9, 2006
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Death
·HEARTWARE, INC·Product code DSQ·September 25, 2015
SPECTRA OPTIA
FDA Adverse Event
Injury
·TERUMO BCT·Product code LKN·July 13, 2023
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·June 8, 2010
HEMOCHRON JR SIGNATURE SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code JPA·March 9, 2011
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·March 27, 2012
HEMOCHRON JR SIGNATURE SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code JPA·March 9, 2011
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·August 17, 2011
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GJS·March 30, 2012
EKOS ENDOVASCULAR DEVICE, 135X30CM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code QEY·May 21, 2026
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·September 6, 2013
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GJS·July 13, 2011
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORPORATION·Product code GKP·October 19, 2011
INRATIO
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC.·Product code GJS·February 24, 2012
ALARIS
FDA Adverse Event
Malfunction
·ALARIS MEDICAL SYSTEMS·Product code FRN·May 23, 2003
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·May 8, 2012
SPECTRA OPTIA
FDA Adverse Event
Injury
·TERUMO BCT·Product code LKN·May 22, 2020
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·August 24, 2012
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·October 5, 2012
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·June 8, 2022