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Device Problem
Degraded (1153)
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Patient Problem
Insufficient Information (4580)
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Event Date 08/15/2023 |
Event Type
malfunction
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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-1972-2021, z-1973-2021, and z-1974-2021.H3 other text : device not returned to manufacturer.
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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 irritation.There was no report of medical intervention.No additional information can be requested at this time.
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Search Alerts/Recalls
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