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Device Problem
Degraded (1153)
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Patient Problems
Pneumonia (2011); Cough (4457)
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Event Date 08/15/2023 |
Event Type
malfunction
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Event Description
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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 an issue related to a philips cpap device's sound abatement foam.The patient's attorney reporting allegations of pneumonia and cough.No other clinical information or medical interventions were reported.The device has not yet been returned to the manufacturer for investigation.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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Manufacturer Narrative
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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 : the device has not yet been returned to the manufacturer.
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Search Alerts/Recalls
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