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 allegations of cancer/ tracheal tumor and asthma (new or worsening).In addition, the customer reported allegations of nose irritation, dizziness and/or headache, hypersensitivity, gerd and insomnia due to not using the device.The manufacturer was made aware of this complaint through a representative of the customer.Medical intervention was not specified.The manufacture's investigation is ongoing.A follow up report will be submitted when the manufacture's investigation is complete.
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