3,847 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NGT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AVANOS
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC.·Product code KNT·August 18, 2025
SALEM SUMP
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code FEG·January 19, 2017
CORFLO
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC.·Product code KNT·May 20, 2020
LEVIN TUBE
FDA Adverse Event
Death
·DAVOL INC. SUBSIDIARY OF CR BARD INC.·Product code FPD·March 24, 1997
DOBBHOFF 12FR 43IN W STYLET EN
FDA Adverse Event
Injury
·CARDINAL HEALTH·Product code KNT·November 9, 2023
CORFLO
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)·Product code KNT·September 30, 2021
CORFLO NASOGASTRIC NASOINTESTINAL PEDIATRIC FEEDING TUBE WITH STYLET WITH ENFIT
FDA Adverse Event
Injury
·AVANOS MEDICAL, INC.·Product code KNT·May 12, 2022
BARD NASOGASTRIC SUMP TUBE WITH ENFIT
FDA Adverse Event
Malfunction
·C.R. BARD, INC.·Product code BSS·April 20, 2023
TUBES, GASTROINTESTINAL (AND ACCESSORIES)
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC.·Product code KNT·December 23, 2019
CORTRAK® 2 ENTERAL ACCESS SYSTEM (EAS) FEEDING TUBES
FDA Adverse Event
Malfunction
·HALYARD HEALTH·Product code KNT·January 27, 2017
NASOGASTRIC FEED TUBE W/ENFIT
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 22, LLC.·Product code KNT·January 21, 2025
KANGAROO NASOGASTRIC TUBE
FDA Adverse Event
Injury
·COVIDIEN·Product code KNT·November 25, 2013
CORFLO ULTRA NG FEEDING TUBE
FDA Adverse Event
Malfunction
·CORPAK MEDSYSTEMS, INC.·Product code KNT·March 14, 2019
NGT 6FR
FDA Adverse Event
Injury
·Product code BSS·January 7, 2013
CORFLO
FDA Adverse Event
Malfunction
·AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)·Product code KNT·September 9, 2021
CORFLO-ULTRA NG WITH STYLET
FDA Adverse Event
Malfunction
·CORPAK MEDSYSTEMS·Product code KNT·August 2, 2017
CORFLO-ULTRA
FDA Adverse Event
Malfunction
·CORPAK MEDSYSTEMS·Product code FPD·September 9, 2016
COVIDIEN KANGAROO 12 FR 43 INCH NGT
FDA Adverse Event
Injury
·Product code FPD·May 22, 2014
ARGYLE SALEM SUMP TUBE
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FEG·March 6, 2017