147 results
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43ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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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