10,000 results
·
158ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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