7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
M.U.S.T. PEDICLE SCREW SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNT·November 4, 2008
AXON DIGITAL PREAMPLIFIER
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code GWF·July 18, 2013
BD PEGASUS YEL 24GA X 0.75IN PRN-CAP Y
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·January 18, 2024
M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024