8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PLASTIPAK¿ HYPODERMIC SYRINGE LUER LOK¿
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·December 28, 2018
CHURCHILL MEDICAL SYSTEMS
FDA Adverse Event
Malfunction
·CHURCHILL MEDICAL SYSTEMS INC.·Product code FPA·April 22, 2008
LINK ENDO-MODEL ROTATION KNEE JOINT PROSTHESIS WITH POREX SURFACE MODIFICATION
FDA Adverse Event
Injury
·WALDEMAR LINK GMBH & CO. KG·Product code KRO·September 10, 2019
LARYNG-O-JET 160 MG 4 ML
FDA Adverse Event
Injury
·INTERNATIONAL MEDICATION SYSTEMS, LTD·Product code FMF·May 5, 2014
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·October 19, 2012
MONARCH
FDA Adverse Event
Injury
·Product code FTL·August 13, 2010
TANGO INFINITY
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·March 28, 2018
LINK ENDO-MODEL® ROTATION KNEE JOINT PROSTHESIS - CEMENTABLE
FDA Adverse Event
Injury
·WALDEMAR LINK GMBH & CO. KG·Product code KRO·February 1, 2019