4 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PLASTIPAK 20 ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·February 25, 2020
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·January 11, 2013
CE INTERMATE SV 200, 48 PACK,50125
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·November 30, 2010
MYNX ACE 6F/7F VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·ACCESSCLOSURE, INC.·Product code MGB·July 2, 2014