10,000 results · 130ms · Sources: EU EUDAMED, US FDA

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TRILOGY O2

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·December 22, 2016

VELA VENTILATOR

FDA Adverse Event
Malfunction ·CAREFUSION, INC·Product code CBK·December 27, 2016

980 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·October 24, 2016

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·October 26, 2016

ESPRIT VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·October 27, 2016

980 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·November 2, 2016

VELA VENTILATOR

FDA Adverse Event
Malfunction ·CAREFUSION, INC·Product code CBK·November 3, 2016

V200 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·October 25, 2016

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·November 30, 2016

980 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·November 30, 2016

EVITA 4

FDA Adverse Event
Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·December 7, 2016

ESPRIT VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 16, 2016

840 VENTILTOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·December 16, 2016

AVEA VENTILATOR

FDA Adverse Event
Malfunction ·CAREFUSION, INC·Product code CBK·December 2, 2016

UNI-VENT MODEL 731

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code CBK·December 13, 2016

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·December 13, 2016

TRILOGY 202

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·December 13, 2016

UNI-VENT MODEL 731

FDA Adverse Event
Malfunction ·IMPACT PRODUCTS·Product code CBK·December 13, 2016

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·December 5, 2016

HT70

FDA Adverse Event
Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·December 19, 2016