3 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNK JUVEDERM VOLUMA
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·April 9, 2014
SOFTCLIX LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 17, 2007
M2A-MAGNUM MODULAR HEAD 52MM HEAD DIAMETER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·September 26, 2012