6 results
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26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VENOUS BLOODLINE NON-MACHINE SPECIFIC
FDA Adverse Event
Malfunction
·ERIKA DE REYNOSA·Product code FJK·July 22, 1999
VENOUS BLOODLINE NON-MACHINE SPECIFIC
FDA Adverse Event
Injury
·ERIKA DE REYNOSA·Product code FJK·July 22, 1999
BOWEL GRASPER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 27, 2014
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIVISION·Product code FNL·November 10, 2010
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 13, 2012
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·February 7, 2018