103 results · 86ms · Sources: EU EUDAMED, US FDA

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ONE TOUCH

FDA Adverse Event
Injury ·LIFESCAN J & J·Product code NBW·February 8, 2016

GTS STANDARD FMRL STEM SIZE -1

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code OQG·July 21, 2019

GTS STANDARD FEMORAL STEM CEMENTLESS S-1

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code JDI·July 21, 2019

AVALON FM30 FETAL MONITOR

FDA Adverse Event
Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code HGM·February 21, 2023

PREVENA PLUS¿ CUSTOMIZABLE¿ DRESSING

FDA Adverse Event
Injury ·KINETIC CONCEPTS, INC.·Product code OMP·March 21, 2018

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

CRYOSPRAY ABLATION SYSTEM

FDA Adverse Event
Injury ·CSA MEDICAL, INC.·Product code GEH·May 7, 2008

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·May 13, 2026

SYNCHROMED

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 6, 2014

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

UNKN ABSORBABLE FAST-FIX DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code GAT·March 25, 2021

MOSES PULSE

FDA Adverse Event
Injury ·LUMENIS LTD·Product code GEX·May 21, 2026

NAVIGATOR

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KOD·May 21, 2026

UNKN SUSPENSORY FIXATION DEV

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBI·March 23, 2021

UNKNOWN VALVE/SHUNT

FDA Adverse Event
Injury ·MEDTRONIC DOMINICANA·Product code JXG·April 16, 2025

MW5060835

FDA Adverse Event
Injury ·March 8, 2016

UNKNOWN ULNAR COMPONENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDC·February 22, 2018