60 results · 25ms · 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.

ARCHITECT I1000SR

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·August 31, 2022

TRAY 40CM PERMCATH

FDA Adverse Event
Malfunction ·TYCO HEALTHCARE/KENDALL·Product code LFJ·December 22, 2006

SYNCHROMED II

FDA Adverse Event
Other ·MEDTRONIC·Product code LKK·June 12, 2006

FOGARTY

FDA Adverse Event
Other ·EDWARDS LIFESCIENCES·Product code DXE·July 17, 2006

UNK

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·April 20, 2006

INVERNESS EAR PIERCING SYSTEM

FDA Adverse Event
Other ·INVERNESS CORPORATION·Product code JYS·July 25, 2007

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Death ·PHYSIO-CONTROL, INC.·Product code MKJ·September 23, 2010

DEEP BRAIN STIMULATION LEAD

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

DEEP BRAIN STIMULATOR LEAD

FDA Adverse Event
Death ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

DEEP BRAIN STIMULATION LEAD

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

ACCU-CHEK COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 22, 2007

AMPLATZER SEPTAL OCCLUDER

FDA Adverse Event
Malfunction ·AGA MEDICAL CORP.·Product code MLV·January 5, 2007

D-TRONPLUS

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·September 29, 2008

DEEP BRAIN STIMULATION LEAD

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

CONCERTO II CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

INTRINSIC

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

HEART LUNG MACHINE

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 25, 2024

HEART LUNG MACHINE

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·September 27, 2024

MULTI-LINK RX VISION CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·GUIDANT VASCULAR INTERVENTION·Product code MAF·September 20, 2006

FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 20, 2008