8 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP.·Product code MKJ·November 8, 2001
BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code DSQ·February 2, 2000
SCHNEIDER C-THRU FLOPPY CORONARY GUIDEWIRE
FDA Adverse Event
Malfunction
·SCHNEIDER (EUROPE) AG·Product code DQX·March 30, 1998
LOCKING SCREW AXSOS 3 TI 4.0MM / L34MM
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HRS·February 9, 2019
CANCELLOUS SCREW AXSOS 3 TI Ø4.0MM / L22MM / FULL THREAD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HRS·February 9, 2019
CANCELLOUS SCREW AXSOS 3 TI Ø4.0MM / L28MM / FULL THREAD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HRS·February 9, 2019
CANCELLOUS SCREW AXSOS 3 TI Ø4.0MM / L24MM / FULL THREAD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HRS·February 9, 2019
RS SIDE EXP DSTL FMRL LT 15CM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KRO·February 17, 2020