9 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014
CATHETER MOUNT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZO·March 1, 2015
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·August 21, 2014
EMAX 2 PLUS MOTOR
FDA Adverse Event
Malfunction
·DEPUY SNYTHES POWER TOOLS·Product code HBC·May 31, 2013
PERSONAL ALARM LOUD
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·June 15, 2011
C.R.E. BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORK LTD.·Product code KNQ·August 28, 2008
NEOPUFF INFANT RESUSCITATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·April 20, 2016
BD SYRINGE 3ML LL 200 S/C
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 3, 2021