2,212 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·February 25, 2003
HUMAPEN ERGO, BURG-OPAQ/CLEAR CARTRIDGE HOLDER
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·April 7, 2006
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code FMF·August 17, 2005
IMED GEMINI INFUSION PUMP
FDA Adverse Event
Injury
·CARDINAL HELATH, ALARIS PRODUCTS·Product code FRN·April 6, 2009
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 20, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 20, 2013
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·November 16, 2023
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code NSC·April 16, 2004
ITREL 3
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·December 10, 2008
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code NSC·April 8, 2004
ITREL 3
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·December 10, 2008
HUMAPEN ERGRO, TEAL/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·July 26, 2005
ITREL 3
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·December 10, 2008
STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·May 19, 2016
PLM A+ SPANISH DEVICE REMAN RESTART
FDA Adverse Event
Injury
·ICU MEDICAL COSTA RICA LTD.·Product code FRN·May 6, 2025
HUMAPEN ERGO, TEAL, OPAQUE
FDA Adverse Event
Malfunction
·ELI LILLY AND CO.·Product code KZE·June 3, 2005
STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·May 19, 2016
SYNERGY
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 30, 2012
STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·May 19, 2016
ALARIS PUMP MODULE
FDA Adverse Event
Injury
·CAREFUSION CORP·Product code FRN·May 13, 2010