342 results
·
52ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·June 5, 2017
980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·April 22, 2017
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·September 24, 2014
BD PROBETEC ET CT/GC AMPLIFIED DNA ASSAY COL
FDA Adverse Event
Injury
·BD DIAGNOSTICS·Product code LSL·February 23, 2009
BD PROBETEC ET CT/GC AMPLIFIED DNA ASSAY COL
FDA Adverse Event
Injury
·BD DIAGNOSTICS·Product code LSL·February 23, 2009
BBL THIOGLYCOLLATE MEDIUM, ENRICHED WITH VIT
FDA Adverse Event
Injury
·BD DIAGNOSTICS·Product code JSG·June 24, 2008
BD DIRECTIGEN MENINGITIS COMBO TEST KIT
FDA Adverse Event
Injury
·BD DIAGNOSTICS·Product code GTJ·August 7, 2008
EMBLEM S-ICD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWS·July 1, 2022
980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·March 21, 2017
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·September 16, 2016
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·August 30, 2016
980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·July 17, 2017
PURITAN BENNETT
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·August 5, 2015
GHIATAS
FDA Adverse Event
Injury
·BARD PERIPHERAL VASCULAR, INC.·Product code GDF·June 24, 2025
BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBE
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code MDB·March 13, 2012
BBL THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITA
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code JSG·October 31, 2012
PHOENIX PMIC/ID-62 PANEL
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code LON·February 23, 2012
BBL THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITA
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code JSG·October 31, 2012
BBL CRYSTAL ENTERIC/NONFERMENTER ID KIT
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code JSS·March 8, 2013
BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMP
FDA Adverse Event
Injury
·BD DIAGNOSTIC SYSTEMS·Product code MKZ·March 8, 2013