6 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·May 16, 2022
SINOVIAL
FDA Adverse Event
Injury
·IBSA FARMACEUTICI ITALIA SRL·Product code MOZ·April 20, 2020
MONARCH III IOL DELIVERY SYSTEM CARTRIDGE - D
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code KYB·October 22, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 3, 2013
REFOBACIN BC R 1X40 US
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 26, 2024