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Model Number 840 |
Device Problem
Device Inoperable (1663)
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Patient Problem
No Code Available (3191)
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Event Date 05/09/2018 |
Event Type
malfunction
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Manufacturer Narrative
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Device evaluation summary: the field service engineer *fse) evaluated the ventilator; however, the patient circuit and filters had been removed from the ventilator.The fse could not duplicate the reported event.The ventilator passed all testing per manufacturer specifications and was returned to the customer for clinical use.If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that, while in use on a patient, the 840 ventilator had severe occlusion and safety valve open which indicates a loss of ventilation.This occurred while a nebulizer treatment was being performed.The patient was removed from the ventilator and placed on an alternate ventilator.The patient was not harmed or injured as a result of the reported event.
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Search Alerts/Recalls
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