7 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 7, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014
2.0MM ASNIS MICRO, CANNULATED SCREWDRIVER, 2.0MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS FREIBURG·Product code LXH·November 24, 2010
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 7, 2011
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 14, 2017
TSRH® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 9, 2022
TSRH® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 9, 2022