10,000 results
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61ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PLM MICDP NITRO OL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 22, 2014
TECNIS IOL
FDA Adverse Event
Malfunction
·AMO MANUFACTURING NETHERLANDS·Product code MFK·June 19, 2023
TECNIS SIMPLICITY
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code HQL·June 19, 2023
COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·July 25, 2021
CADENCE PHYSION QC ADULT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code MLN·June 17, 2014
EMMETT
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code MKJ·October 11, 2016
LIFEPAK 15
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code MKJ·August 27, 2015
"QUIK-COMBO" - ADULT PACING/DEFIBRILLATION/ECG ELECTRODES
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code LDD·June 17, 2014
LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code MKJ·March 26, 2010
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code LDD·May 28, 2010
LIFEPAK 7
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code HSH·September 20, 1996
LIFEPAK DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code LDD·August 23, 1996
LIFE PAK
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code LDD·July 8, 1996
LIFE PAK
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code LDD·July 22, 1996
LIFE PAK 500
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code MKJ·December 4, 2014
PHYSIO CONTROL
FDA Adverse Event
Malfunction
·PHYSIO CONTROL·Product code MLN·August 8, 2000
LIFEPAK
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code LDD·January 10, 1994
LIFEPACK 8 QUICK PACE CASSETTE
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code LDD·February 15, 1994
PHYSIO-CONTROL LIFEPAK 90
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code LDD·April 4, 2000
JOLIFE
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL·Product code DRM·December 21, 2009