10,000 results · 158ms · 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.

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 21, 2014

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 29, 2005

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 2, 2004

PUMP,INSULIN,512 NA SMOKE

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code LZG·June 11, 2004

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 10, 2006

COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·January 23, 2006

MX-PRO R-3 AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code INK·October 8, 2012

MA204

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·December 19, 2012

ARIS TRANS-OBTURATOR

FDA Adverse Event
Injury ·COLOPLAST A/S·Product code FTL·October 7, 2013

R SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 22, 2013

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·December 19, 2012

ARIS TRANS-OBTURATOR

FDA Adverse Event
Injury ·COLOPLAST MANUFACTURING US, LLC·Product code FTL·October 7, 2013

WECK AUTO ENDO5 ML

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code GDO·June 26, 2014

ECG ELECTRODES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 23, 2013

ARIS TRANS-OBTURATOR

FDA Adverse Event
Injury ·COLOPLAST A/S·Product code FTL·October 7, 2013

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 21, 2014

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 28, 2013

CPR STAT PADS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MLN·March 17, 2014

ACRYSOF

FDA Adverse Event
Malfunction ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·October 1, 2010

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code NVZ·August 12, 2023