8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AIRVANCE BONE SCREW (REPOSE) SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRK·March 3, 2014
AIRVANCE BONE SCREW (REPOSE) SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code LRK·March 29, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 11, 2013
FUSION NAVIGATION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·December 28, 2010
UNKNOWN HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 28, 2014
AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRK·November 30, 2015
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·March 24, 2025
AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code LRK·October 2, 2015