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.Received.The patient has alleged lung disease,nose irritation,respiratory tract irritation,pinflammatory response,colon cancer,cardiopulmonary response.There was no report of patient harm or injury.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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