9,434 results · 39ms · Sources: EU EUDAMED, US FDA

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COMPLETE SE ILIAC

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIO·November 5, 2014

PIPELINE

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 29, 2024

PIPELINE

FDA Adverse Event
Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 29, 2024

OLYMPUS AU400 CLINICAL CHEMISTRY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER MISHIMA K.K.·Product code JJE·December 6, 2011

COMPLETE SE ILIAC

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIO·November 5, 2014

UNICEL® DXC 600 SYNCHRON® SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·September 28, 2011

ZIMMER HIP IMPLANT

FDA Adverse Event
Injury ·ZIMMER·Product code KWA·February 28, 2017

CLOSED APHERESIS KIT, PL3014, SAMPLE POUCH AMS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP.·Product code GKT·April 8, 1997

COMPLETE SE ILIAC

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIO·November 5, 2014

COMPLETE SE ILIAC

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code NIO·November 5, 2014

COMPLETE SE ILIAC

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIO·November 5, 2014

ASR ACETABULAR CUPS 56

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·June 29, 2012

HORIZON TI ML 6/CART 120/BOX

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code FZP·March 26, 2026

ASR UNI FEMORAL IMPL SIZE 47

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·November 28, 2011

ASR ACETABULAR CUPS 54

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·November 28, 2011

ACCU-CHEK ® COMPACT PLUS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·February 26, 2010

UNKNOWN HIP FEMORAL STEM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·April 27, 2021

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 30, 2012

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·October 13, 2009

UNKNOWN DEPUY ASR FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·March 12, 2012