9 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HUDSON AQUAPAK 340 SW, 340 ML W/040 ADAPTOR
FDA Adverse Event
Malfunction
·TELEFELX MEDICAL·Product code BTT·March 2, 2015
DINAMAP PROCARE SERIES MONITOR
FDA Adverse Event
Malfunction
·GE HEALTHCARE·Product code MWI·September 9, 2010
DINAMAP PROCARE SERIES MONITOR
FDA Adverse Event
Malfunction
·GE HEALTHCARE·Product code MHX·September 9, 2010
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·June 9, 2022
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Death
·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·June 9, 2022
UNKNOWN DEPUY 12.5MM PS TIB INSERT
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·March 21, 2013
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Death
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·June 9, 2022