73 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
K-WIRE 1.1, 100MM
FDA Adverse Event
Malfunction
·TRIMED INC·Product code NDL·October 22, 2021
TORX 8 DRIVER, 110MM NIPPLE TIP
FDA Adverse Event
Malfunction
·TRIMED, INC.·Product code HXX·December 4, 2024
FOLEY CATHETER, ADULT 400 SERIES, 16 FR.
FDA Adverse Event
Malfunction
·MRI MEDICAL INC.·Product code KOD·January 9, 2009
PRIMED INSTRUMENTATION INC
FDA Adverse Event
Malfunction
·PRIMED INSTRUMENTS INC·Product code KNW·March 26, 2002
FOLEY CATHETER, ADULT 400 SERIES, 16 FR.
FDA Adverse Event
Malfunction
·MRI MEDICAL INC.·Product code KOD·December 18, 2008
*
FDA Adverse Event
Malfunction
·MRI MEDICAL INC.·Product code KOD·November 12, 2008
FOLEY CATHETER, ADULT 400 SERIES, 16 FR.
FDA Adverse Event
Malfunction
·MRI MEDICAL INC.·Product code KOD·September 18, 2008
PEG EXTENDER
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 20, 2017
WRIST HOOK DORSAL IMPACTOR
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 14, 2017
PEG EXTENDER
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 20, 2017
HEX DRIVER 2.5MM AO; HEX DRIVER 3.5 AO
FDA Adverse Event
Malfunction
·TRIMED INC.·Product code HWR·December 11, 2017
HEX DRIVER 2.5MM AO
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code HWC·December 11, 2017
PEG EXTENDER
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 20, 2017
WRIST HOOK DORSAL IMPACTOR
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 14, 2017
PEG EXTENDER
FDA Adverse Event
Malfunction
·TRIMED, INC·Product code LXH·December 20, 2017
QUICK GUIDE, 1.8MM
FDA Adverse Event
Malfunction
·TRIMED INC·Product code LXH·September 7, 2021
1ST MTP 0 DEGREE DORSIFLEXED,LT,9-HOLE
FDA Adverse Event
Malfunction
·TRIMED INC·Product code HRS·April 12, 2022
VOLAR BEARING PLATE, 3-HOLE, LT
FDA Adverse Event
Malfunction
·TRIMED INC·Product code HRS·August 29, 2025
LOCKING PLATE, CURVED A, 8-HOLE
FDA Adverse Event
Malfunction
·TRIMED, INC.·Product code HRS·October 19, 2018
SAW GUIDE A, 2MM
FDA Adverse Event
Malfunction
·TRIMED, INC.·Product code LXH·October 22, 2025