23 results · 35ms · Sources: EU EUDAMED, US FDA

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K-WIRE GAMMA Ø3,2X450 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 20, 2016

K-WIRE GAMMA Ø3,2X450 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 20, 2016

UNKNOWN

FDA Adverse Event
Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DTK·August 20, 2014

ZOOM

FDA Adverse Event
Malfunction ·EXTERNAL MANUFACTURER·Product code KRG·April 9, 2013

EASYPUMP

FDA Adverse Event
Malfunction ·I-FLOW CORPORATION·Product code MEB·February 24, 2011

CONTAK RENEWAL 4

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

GUNTHER TULIP VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·April 3, 2026

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·December 5, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·November 1, 2017

GUNTHER TULIP VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·November 4, 2025

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·February 27, 2018

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·May 5, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·May 12, 2017

UNKNOWN

FDA Adverse Event
Injury ·Product code DTK·August 20, 2020

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 26, 2014

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·October 26, 2022

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·August 24, 2016