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    FLEXI-Q DV AND DVR AUTO-INJECTORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOME LIQUID OXYGEN DEVICE

    FDA Adverse Event
    Malfunction ·CAIRE, INC.·Product code CAW·November 9, 1995

    COMPANION 31T

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·May 28, 2020

    LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·July 9, 2019

    LIBERATOR

    FDA Adverse Event
    Injury ·CAIRE INC·Product code BYJ·April 8, 2026

    LIBERATOR 45

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·February 3, 2016

    CAIRE LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE, INC.·Product code BYJ·March 13, 2014

    CAIRE

    FDA Adverse Event
    Injury ·CAIRE, INC.·Product code BYJ·September 16, 2013

    CAIRE LIBERATOR 45

    FDA Adverse Event
    Injury ·CAIRE, INC.·Product code BYJ·October 11, 2013

    LIBERATOR

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·May 31, 2023

    CLAIRE LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE, INC.·Product code BYJ·July 22, 2014

    LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·May 20, 2019

    LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·July 9, 2019

    STROLLER

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code BYJ·June 23, 2020

    STROLLER

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·February 8, 2019

    HELIOS U46

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·April 23, 2020

    LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·September 5, 2019

    CAIRE LIBERATOR 30

    FDA Adverse Event
    Malfunction ·CAIRE, INC.·Product code BYJ·March 24, 2014

    HELIOS RESERVOIR

    FDA Adverse Event
    Injury ·CAIRE, INC.·Product code BYJ·March 26, 2015

    LIBERATOR 45

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code BYJ·June 23, 2020