81 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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NEXGEN FEMORAL COMPONENT OPTION FOR CEMENTED USE ONLY SIZE E LEFT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
PERSONA ARTICULAR SURFACE WITH HINGE POST EXTENSION SIZE E 20 MM HEIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
PERSONA ARTICULAR SURFACE WITH SEGMENTAL HINGE POST SIZE E 20 MM HEIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
RIGHT SIZE E CEMENTED OPTION FEMORAL COMPONENT FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2023
NEXGEN FEMORAL AUGMENTS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018
NEXGEN FEMORAL AUGMENTS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018
RICHARD ALLEN SURGICAL NEEDLE
FDA Adverse Event
Other
·ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·February 21, 2013
ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·February 15, 2011
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code LWP·August 7, 2014
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 9, 2016
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
ADAPTA D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
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