16 results
·
17ms
·
Sources: EU EUDAMED, US FDA
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVAMEX·Product code FSA·August 6, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·July 25, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·July 23, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVAMEX·Product code FNG·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·July 29, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code FNG·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·July 22, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FNG·July 24, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·July 31, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·August 12, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVAMEX·Product code FNG·August 2, 2013
ARTERIAL CATHETER KIT
FDA Adverse Event
Injury
·ARGON MEDICAL DEVICES INC.·Product code GDY·February 19, 2019
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MGB·July 18, 2019