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Model Number DSX500T11C |
Device Problem
Degraded (1153)
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Patient Problems
Headache (1880); Vertigo (2134); Dizziness (2194)
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Event Date 07/13/2021 |
Event Type
malfunction
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Manufacturer Narrative
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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 patient has alleged that dizzy upon waking & headaches started worsening june, balance issues last year and went for physical therapy which helped, then had vertigo issues and back to physical therapy that for a while doesn't sleep well without device either was a chemist at dupont and very curious of the chemical reactions.Patient seeks medical intervention for vestibular testing.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 previously 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 patient has previously alleged that dizzy upon waking & headaches started worsening june, balance issues last year and went for physical therapy which helped, then had vertigo issues and back to physical therapy that for a while doesn't sleep well without device either was a chemist at dupont and very curious of the chemical reactions.Patient seeks medical intervention for vestibular testing.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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