4 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·March 5, 2018
ARGON 28 GAUGE SPLITTABLE NEEDLE INTRODUCER
FDA Adverse Event
Malfunction
·ARGON MEDICAL DEVICES, INC·Product code LJS·January 16, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
EXP TIBIAL INSERTS AND PATELLAR COMPONENTS
FDA Adverse Event
Malfunction
·STELKAST, INC·Product code JWH·July 9, 2014