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Model Number DSX500T11C |
Device Problem
Degraded (1153)
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Patient Problems
Excessive Tear Production (2235); Sore Throat (2396); Respiratory Tract Infection (2420); Unspecified Respiratory Problem (4464); Unspecified Eye / Vision Problem (4471)
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Event Date 11/11/2021 |
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, and mechanical ventilator devices.The manufacturer received information alleging runny eye, cloudy eye, stuff nose, nasal irritation, throat soreness.There was no report of serious or permanent patient harm or injury.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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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 previously received information alleging visualization of particles related to a cpap device's sound abatement foam.There was no report of patient harm or injury.After the first/second attempt to have the device and components returned for evaluation, the customer stated that the device will not be returned.The manufacturer is submitting a final report at this time.If pertinent information becomes available to the manufacturer at a later date, an addendum to this final report will be filed.Section h6 updated in this report.
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Search Alerts/Recalls
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