5 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
K883239
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·August 24, 2009
CAPD DISP DISCONNECT, UV FLASH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code KDJ·May 23, 2008
MAYFIELD 2000 SKULL CLAMP
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES CORP. (INTEGRA-OHIO)·Product code HBL·October 20, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 7, 2014
MATRIX POLYAXIAL SCREW
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·December 21, 2012