4 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 21, 2019
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012
INRATIO
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INCORPORATED·Product code GJS·August 20, 2010