Since no device information was provided, the exact recall number is unknown.Possible recall numbers include z-1972,z-1973, and z-1974.H3 other text : device not returned to manufacturer.
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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 and/or headache, nausea / vomiting, asthma.No medical intervention was specified by the patient.The device has not yet been returned to the manufacturer for evaluation.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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