51 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

UNK LIQUID EMBOLIC

FDA Adverse Event
Death ·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021

UNK LIQUID EMBOLIC

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 8, 2017

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 22, 2013

UNK - RODS: VIPER

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·April 9, 2026

UNK - CONSTRUCTS: VIPER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·April 9, 2026

UNKNOWN GEL IMPLANTS

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·February 12, 2026

SUTURE, ABSORBABLE, SYNTHETIC

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·September 5, 2019

SD01 65/18

FDA Adverse Event
Injury ·BIOTRONIK SE & CO. KG·Product code NVN·April 29, 2014

SD01 65/16

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·October 29, 2014

SD01 65/16

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·May 26, 2021

J201 PROTIME CUVETTES

FDA Adverse Event
Malfunction ·INTERNATIONAL TECHNIDYNE CORP·Product code JPA·November 2, 2006

ABBOTT M2000

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code JJH·December 16, 2011

NV GXL LINER NEUTRAL, 40MM ID, GROUP 3 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·May 8, 2024

CC TIBIAL INSERT SZ 1D, 15MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 22, 2024

ACRYSOF IQ TORIC

FDA Adverse Event
Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·February 16, 2011

ALTEON HIP COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code LPH·October 16, 2025

STRAIGHT ATTACHMENT PERFORATOR DRIVER LEGEND AD01

FDA Adverse Event
Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·August 5, 2003