6 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PEN NDL 32G 4MM PRO 90CT US
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·October 22, 2024
PEN NDL 32G 4MM PRO 90CT US
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 23, 2024
PEN NDL 32G 4MM PRO 90CT US
FDA Adverse Event
Malfunction
·BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND·Product code FMI·April 9, 2024
ENERGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 11, 2013
CUSTOM PAK
FDA Adverse Event
Injury
·ALCON - HOUSTON·Product code KYG·April 8, 2011
AUTOCAT 2 WAVE JAPANESE
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC·Product code DSP·May 22, 2008