Device Problem
Leak/Splash (1354)
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Patient Problem
No Patient Involvement (2645)
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Event Date 03/08/2018 |
Event Type
malfunction
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Manufacturer Narrative
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Ge healthcare¿s investigation into the reported occurrence is ongoing.A follow-up report will be issued when the investigation has been completed.No report of patient involvement.Date of device manufacture was unavailable at time of mdr filing.Device evaluation anticipated, but not yet begun.
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Event Description
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The hospital reported a leak from the valve block.There was no report of patient involvement.
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Manufacturer Narrative
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Additional information was received stating that there was a leak but it was less than 9l/min which would not interrupt mechanical ventilation.This was not a reportable malfunction.Additional information was received stating that there was a leak but it was less than 9l/min which would not interrupt mechanical ventilation.This was not a reportable malfunction.
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Search Alerts/Recalls
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