1,783 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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PRECISION 500D
FDA Adverse Event
Injury
·GE MEDICAL SYSTEMS, INC.·Product code JAA·August 18, 2017
SMARTPORT CT/TI/POLY 8F
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC.·Product code LLD·February 10, 2023
MONORAIL
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·November 22, 2015
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·November 6, 2008
UNKNOWN ACETABULAR CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·October 23, 2017
DUROM ACETABULAR COMPONENT
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·August 8, 2011
HARMONIC SCALPEL CURVED SHEAR (EXACT CODE UNKNOWN)
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·January 17, 2020
DUROM ACETABULAR COMPONENT 56/50 CODE P
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·October 24, 2011
DUROM ACETABULAR COMPONENT 56/50 CODE P
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·October 26, 2011
ACCUTRAK DELIVERY CATHETER SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·February 9, 2021
DUROM HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·October 13, 2011
HARMONIC ACE 5MM SHEAR
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 23, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·April 9, 2013
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·April 26, 2024
DUROM US ACETABULAR COMPONENT 50/44 J
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·September 22, 2011
DUROM US ACETABULAR COMPONENT 48/42 H
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·August 8, 2011
INTELLIS
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·May 21, 2021
LOTUS VALVE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NPT·May 13, 2021
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·July 28, 2020
RIPTIDE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 9, 2024