5 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CONTAK RENEWAL 3
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code NIK·November 11, 2008
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·August 11, 2011
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·February 20, 2018
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·April 18, 2018
LASER PROBES
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQE·April 21, 2017