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 congestive heart failure, kidney failure, and low blood pressure.In addition, the device will not turn on/device not functioning.Medical intervention was hospitalization.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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