26 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
9616026-2006-00240
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616026-2006-00244
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
ORTHOPEDIATRICS PEDIFRAG SYSTEM 3.5MM, 2.0MM DRILL BIT
FDA Adverse Event
Malfunction
·ORTHOPEDIATRICS·Product code HRS·July 22, 2016
BD NEEDLE ECLIPSE 25X5/8
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 28, 2024
BD NEEDLE ECLIPSE 25X5/8
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 28, 2024
BD NEEDLE ECLIPSE 25X5/8
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 28, 2024
BD NEEDLE ECLIPSE 25X5/8
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 28, 2024
BD NEEDLE ECLIPSE 25X5/8
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 28, 2024
9616026-2006-00239
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00222
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00252
FDA Adverse Event
Other
·Product code FII·June 21, 2006
9616026-2006-00245
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00253
FDA Adverse Event
Other
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00221
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SETS (M)
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024
OMNIPOD 5 POD
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code QFG·November 7, 2024