60 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
ARROW
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023
CODMAN 3000
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023
CODMAN 3000
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023
CODMAN
FDA Adverse Event
Death
·CODMAN & SHURTLEFF·Product code LKK·July 18, 2023
BIOCOMP. INTERFERENCE SCREW, FULL THREAD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MAI·June 24, 2014
ENDO GIA UNIVERSAL 12MM SINGLE USE INST
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·November 1, 2010
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Death
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·November 10, 2014
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 5, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 6, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015