Update from the Food and Drug Agency comes days after Philips said it would stop selling the devices in the U.S.

FDA says 561 deaths tied to recalled Philips sleep apnea machines::Update from the Food and Drug Agency comes days after Philips said it would stop selling the devices in the U.S.

  • Whirling_Cloudburst@lemmy.worldEnglish
    47·
    10 months ago

    More info is needed. Here ya go folks:

    Philips recalled the following devices made between 2009 and April 26, 2021:

    A-Series BiPAP A30
A-Series BiPAP A40 (ventilator)
A-Series BiPAP Hybrid A30
A-Series BiPAP V30 Auto (ventilator)
C-Series ASV (ventilator)
C-Series S/T and AVAPS
DreamStation
DreamStation ASV
DreamStation Go
DreamStation ST, AVAPS
Dorma 400
Dorma 500
E30
Garbin Plus, Aeris, LifeVent (ventilator)
OmniLab Advanced+
REMstar SE Auto
SystemOne ASV4
SystemOne (Q-Series)
Trilogy 100 (ventilator)
Trilogy 200 (ventilator)

    Sauce