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Model Number DSXHCP |
Device Problem
Degraded (1153)
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Patient Problems
Sinus Perforation (2277); Unspecified Respiratory Problem (4464)
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Event Date 10/12/2023 |
Event Type
malfunction
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Manufacturer Narrative
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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 sinus allergies and breathing issues.There was no serious patient harm or injury.No medical intervention was specified by the patient. the device has not yet been returned to the manufacturer for evaluation.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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Search Alerts/Recalls
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