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Model Number DSX400H11C |
Device Problem
Degraded (1153)
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Patient Problems
Abdominal Pain (1685); Dyspnea (1816); Pain (1994); Sore Throat (2396); Respiratory Tract Infection (2420); Cough (4457); Dry Mouth (4485)
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Event Date 04/11/2022 |
Event Type
malfunction
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Event Description
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The manufacturer received information alleging cough, dry throat, difficulty breathing, back pain, stomach pain, nasal/throat irritation or soreness, particles in tubing/chamber related to a cpap device's sound abatement foam.There was no report of serious 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 reported an allegation of particles in tubing//chamber related to a cpap device's sound abatement foam.The manufacturer received information alleging cough, dry throat, difficulty breathing, back pain, stomach pain.There was no report of serious or permanent harm or injury.The device was returned to the manufacturer's service center for further evaluation.The device was evaluated.There was no mention of visual findings to the external part of the device.The internal aspect of the device was inspected.The device powered on and airflow was confirmed.The device's downloaded logs were reviewed by the manufacturer.There were 0 errors found.The manufacturer concludes that they could not confirm the customer's allegation and there was no visible foam degradation and unit scrapped due to 400 model.Section h6 updated in this report.
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Search Alerts/Recalls
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