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 cpap device's sound abatement foam.The patient alleged has not slept well since last (july of 2021), waking up several times a night and feeling exhausted all day long.Patient stated headaches and exhaustion are constant.There was no report of serious or permanent patient harm or injury.The manufacture's investigation is ongoing.A follow up report will be submitted when the manufacture's investigation is complete.
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