9 results
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37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 7, 2021
5MM MINI PEN NEEDLE
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMI·January 22, 2007
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013
ARCHITECT HIV AG/AB COMBO
FDA Adverse Event
Death
·ABBOTT·Product code MZF·March 28, 2011
ACCU-CHEK MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·April 21, 2008
OPTETRAK ASY,CR CEMENTED FEMORAL, SZ 2,
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 25, 2024
INSET PATELLA 26MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 25, 2024
UNKNOWN EMPRINT ANTENNA
FDA Adverse Event
Injury
·COVIDIEN LP - SUPERDIMENSION INC·Product code LLZ·January 4, 2023
UNKNOWN COOL TIP ELECRTRODE
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·January 5, 2023