10 results
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52ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
ENTERAL FEEDING TUBE WITH STYLET
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code FPD·December 30, 2014
CORTRAK 2 EAS
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code KNT·March 6, 2014
CORTRAK 2 EAS ELECTROMAGNETIC TRANSMITTING STYLET AND CORFLO FEEDING TUBE
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code KNT·January 26, 2017
CORTRAK 2
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code KNT·April 30, 2019
CORTRAK ENTERAL ACCESS
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code KNT·May 26, 2017
CORFLO ENTERAL FEEDING TUBE
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC.·Product code KNT·January 24, 2025
CORFLO MAX PEG KIT
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS INC·Product code KNT·June 15, 2015
CORFLO-ULTRA LITE
FDA Adverse Event
Injury
·CORPAK MED SYSTEMS, INC.·Product code FPD·September 13, 2001
CORLITE ENTERAL FEEDING TUBE WITH ENFIT CONNECTOR
FDA Adverse Event
Injury
·CORPAK MEDSYSTEMS, INC. / MEDICAL INDUSTRIES, INC.·Product code KNT·July 11, 2019
CORTRAK
FDA Adverse Event
Injury
·CORPAK MED SYSTEMS / AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)·Product code KNT·September 7, 2022