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 dizziness, headaches, "kidney damage, cyst on kidney, and breathing problems" response.The manufacturer was made aware of this complaint through a representative of the customer.Medical intervention was not specified.No other information has been received however if additional information is received a supplemental/follow up will be sent.
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