The manufacturer was contacted in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging an issue related to a dream station bipap autosv device's sound abatement foam.The patient has alleged device shut off it was alarming with message system malfunction and experienced not sleeping well and very tired during exercise.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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