342 results · 52ms · Sources: EU EUDAMED, US FDA

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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