27 results · 24ms · Sources: EU EUDAMED, US FDA

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AU680 CHEMISTRY ANALYZER WITH ISE

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 14, 2013

XACT CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA·Product code NIM·December 3, 2010

PINN SECTOR W/GRIPTION 54MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 3, 2014

UNI GLENOID-PERIPHERAL LOCK SCRW

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

UNIVERSAL GLENOID - BASEPLATE SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

UNI GLENOID-PERIPHERAL LOCK SCRW

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·December 21, 2020

UNIVERSAL GLENOID - BASEPLATE SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

UNIVERS REVERS GLENOSPHERE 36 +2.5 INF

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·April 4, 2019

HUMERAL INSERT S/36 +3 TO FIT IN 36 CUP

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

UNIVERS REVERS SUTURE CUP, 36 (+2 RIGHT)

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HSD·April 4, 2019

UNI GLENOID-PERIPHERAL LOCK SCRW

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

UNIVERS REVERS HUMERAL STEM, SIZE 6

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HSD·April 4, 2019

1220246-2019-01001

FDA Adverse Event
Injury ·April 4, 2019

HUMERAL INSERT S/36 +6 TO FIT IN 36 CUP

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·April 4, 2019

1220246-2019-01005

FDA Adverse Event
Injury ·April 4, 2019

UNI GLENOID-PERIPHERAL LOCK SCRW

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·September 10, 2020

UNIVERS REVERS GLENO 42 +4 LAT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·August 5, 2019

UNI GLENOID-PERIPHERAL LOCK SCRW

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

ECLIPSE CAGE SCREW S, 30MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·March 10, 2020

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·March 10, 2020