1,049 results · 29ms · Sources: EU EUDAMED, US FDA

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K-WIRE / DZK

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code DZK·May 11, 2009

HA COATED HALF PINS

FDA Adverse Event
Injury ·SMITH & NEPHEW·Product code DZK·May 5, 2014

UNKNOWN TOGGLELOC

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code DZK·October 11, 2021

PINS/WIRES

FDA Adverse Event
Injury ·SYNTHES USA·Product code DZK·May 3, 2012

CABLE/WIRE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code DZK·May 10, 2012

PINS/WIRES

FDA Adverse Event
Injury ·Product code DZK·June 4, 2012

K-WIRE

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZK·September 17, 2003

K-WIRES

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZK·September 17, 2003

UNK

FDA Adverse Event
Other ·UNK·Product code DZK·August 25, 2003

TRUE/LOK EXTERNAL FIXATION SYSTEM WIRE

FDA Adverse Event
Malfunction ·ORTHOFIX INC.·Product code DZK·November 13, 2008

PINS/WIRES

FDA Adverse Event
Injury ·SYNTHES USA·Product code DZK·December 13, 2012

WIRE

FDA Adverse Event
Injury ·Product code DZK·October 5, 2012

WIRE/PIN

FDA Adverse Event
Injury ·SYNTHES USA·Product code DZK·November 9, 2012

K-WIRE 10/10 - LENGTH 70 MM

FDA Adverse Event
Malfunction ·INTEGRA, SAINT PRIEST·Product code DZK·April 8, 2011

2.8MM THREADED GUIDE WIRE 450MM/TROCAR POINT

FDA Adverse Event
Malfunction ·Product code DZK·February 27, 2013

WIRE, FIXATION, INTRAOSSEOUS

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code DZK·November 27, 2018

WIRE BAY PT CORTICAL 370MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code DZK·February 27, 2013

WIRE, FIXATION, INTRAOSSEOUS

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code DZK·March 7, 2014

CORE IMPACTION DRILL

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZK·February 7, 2014

SMOOTH WIRES

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code DZK·June 27, 2013