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 prostate cancer, pulmonary damage and inflammatory response while using the device.Medical intervention was not specified.No additional information can be requested at this time.This device is not in scope of the uno remediation but is included in the same allegations of harm by the same patient for multiple devices which are in scope of the uno recall.Related ra 317712360, 317712358.The manufacturer was made aware of this complaint through a representative of the customer.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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