8 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FASTTAKE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·November 21, 2001
DREAMSTATION BIPAP PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·November 6, 2024
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·July 29, 2011
6000CMS
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 14, 2013
INTERSTIM
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·September 26, 2008
NEEDLE 26X1/2 RB
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 9, 2020
BAB TOUGH STRIPS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON CONSUMER INC.·Product code KGX·April 22, 2021
EXEL HYPO NDL 27GX1-1/4"
FDA Adverse Event
Injury
·EXELINT INTERNATIONAL, CO.·Product code FMF·March 25, 2024