Model Number DSX520H11C |
Device Problem
Increase in Pressure (1491)
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Patient Problems
Asthma (1726); Chest Pain (1776); Respiratory Tract Infection (2420)
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Event Date 01/26/2024 |
Event Type
Injury
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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 cpap device's sound abatement foam.The patient has alleged to chest pain, lung infection, presure high and asthma.Medical intervention was specified.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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H3 other text : device not returned to manufacturer.
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Manufacturer Narrative
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The manufacturer was contacted in reference to ds2adv auto cpap.Device.The patient has alleged to chest pain, lung infection, pressure high and asthma.Medical intervention was specified.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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Event Description
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The manufacturer was contacted in reference to ds2adv auto cpap.Device.The patient has alleged to chest pain, lung infection, pressure high and asthma.Medical intervention was specified.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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