Model Number 1006-9321-000 |
Device Problem
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
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For the reported event, a ge healthcare service representative and hospital biomed engineer performed a checkout of the system and confirmed the reported event.The circuit identification board was replaced to resolve the reported issue.
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Event Description
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This report summarizes 1 malfunction event.A review of the event indicated that model 1006-9321-000 anesthesia gas machine experienced a flow sensor error causing a loss of mechanical ventilation.The report was received from a single source.The reported event did not involve a patient.
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Search Alerts/Recalls
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