12 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ANIMAS VIBE SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code OYC·September 3, 2015
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·January 13, 2014
ACRYSOF IQ TORIC
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·August 2, 2013
DIMENSION XPAND PLUS WITH HM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·October 27, 2014
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 3, 2011
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 26, 2013
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON- RESEARCH LTD/HUNTINGTON·Product code HQL·December 10, 2013
INTRALASE
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code HNO·April 6, 2016
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 15, 2022
ACRYSOF RESTOR
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013
UNSPECIFIED SYSTEM
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQC·September 17, 2013