5 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BD VERITOR ¿ AT-HOME COVID-19 TEST
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·August 3, 2022
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·May 28, 2025
GYNECARE MORCELLEX* TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·April 2, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 4, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008