147 results · 43ms · Sources: EU EUDAMED, US FDA

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ONX AORTIC CONFORM EXT 21

FDA Adverse Event
Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·December 23, 2024

ONX ASCENDING AORTIC 27/29

FDA Adverse Event
Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·June 18, 2024

BIOGLUE SYRINGE 5-PACK, 10ML, JAPAN

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·May 23, 2024

PHOTOFIX PATCH - 6CM X 8CM

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code DXZ·December 23, 2024

BIOGLUE- UNKNOWN CONFIGURATION

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·April 26, 2024

ONX MITRAL CONFORM 25/33

FDA Adverse Event
Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·July 6, 2023

BIOGLUE

FDA Adverse Event
Death ·ARTIVION, INC.·Product code MUQ·July 16, 2024

BIOGLUE SYRINGE 5-PACK, 5ML, G

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·July 10, 2024

PULMONARY VALVE & CONDUIT SG

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code OHA·February 17, 2023

PULMONARY VALVE & CONDUIT

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MIE·August 23, 2024

PULMONARY VALVE & CONDUIT SG

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code OHA·September 8, 2023

BIOGLUE SYRINGE 5-PACK, 10 ML, JAPAN

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·March 29, 2023

ONX MITRAL CONFORM 25/33

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code LWQ·October 6, 2025

BIOGLUE SYRINGE 5-PACK, 2ML

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·December 23, 2025

BIOGLUE-UNKNOWN CONFIGURATION

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·November 10, 2025

PHOTOFIX UNKNOWN CONFIGURATION

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code PSQ·November 12, 2025

BIOGLUE SURGICAL ADHESIVE

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·December 3, 2025

BIOGLUE SYRINGE 5-PACK, 5ML

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·December 23, 2025

BIOGLUE SYRINGE 5-PACK, 10 ML, JAPAN

FDA Adverse Event
Injury ·ARTIVION, INC.·Product code MUQ·August 14, 2023

1063481-2011-00055

FDA Adverse Event
Injury ·ARTIVION, INC.·August 12, 2011