51 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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UNK LIQUID EMBOLIC
FDA Adverse Event
Death
·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021
UNK LIQUID EMBOLIC
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·September 8, 2017
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 22, 2013
UNK - RODS: VIPER
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·April 9, 2026
UNK - CONSTRUCTS: VIPER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·April 9, 2026
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·February 12, 2026
SUTURE, ABSORBABLE, SYNTHETIC
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·September 5, 2019
SD01 65/18
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·April 29, 2014
SD01 65/16
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·October 29, 2014
SD01 65/16
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code LWS·May 26, 2021
J201 PROTIME CUVETTES
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP·Product code JPA·November 2, 2006
ABBOTT M2000
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code JJH·December 16, 2011
NV GXL LINER NEUTRAL, 40MM ID, GROUP 3 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·May 8, 2024
CC TIBIAL INSERT SZ 1D, 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 22, 2024
ACRYSOF IQ TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·February 16, 2011
ALTEON HIP COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code LPH·October 16, 2025
STRAIGHT ATTACHMENT PERFORATOR DRIVER LEGEND AD01
FDA Adverse Event
Malfunction
·MEDTRONIC MIDAS REX·Product code HBB·August 5, 2003