6 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·October 6, 2017
MWA PERCUTANEOUS ANTENNA 22CM
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code NEY·November 18, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 14, 2014
VERSACARE BED
FDA Adverse Event
Other
·HILL-ROM, INC.·Product code FNL·December 19, 2012