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 cancer and new or worsening of asthma.The manufacturer was made aware of this complaint through a representative of the customer.Medical intervention was not specified.The device has not yet been returned to the manufacturer for evaluation and there is no contact information to gain additional information on the device.At this time, no further investigation can be performed.If any additional information is received, a follow up report will be filed.
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