RESPIRONICS, INC. DREAMSTATION BIPAP AUTOSV; VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING
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Model Number DSX900H11C |
Device Problem
Degraded (1153)
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Patient Problems
Dry Eye(s) (1814); Headache (1880); Sneezing (2251); Sore Throat (2396); Respiratory Tract Infection (2420); Unspecified Ear or Labyrinth Problem (4474)
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Event Date 12/17/2021 |
Event Type
malfunction
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Event Description
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The manufacturer received information alleging an issue related to a bipap device's sound abatement foam.The patient alleged nasal/throat irritation or soreness, sore throat, ear irritation, sneezing problems, headaces, eyes bothering.There was no report of serious 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 an issue related to a bipap device's sound abatement foam.The patient alleged nasal/throat irritation or soreness, sore throat, ear irritation, sneezing problems, headaches, eyes bothering.There was no report of patient harm or injury.Repeated attempts to have the device and components returned for evaluation and investigation were unsuccessful.The manufacturer believes they will be unable to gather additional information. 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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