Catalog Number 0250070600 |
Device Problems
Mechanical Problem (1384); Suction Problem (2170)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 04/20/2020 |
Event Type
malfunction
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Manufacturer Narrative
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Additional information will be provided once the investigation has been completed.
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Event Description
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It was reported that there was loss of insufflation during a case.
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Manufacturer Narrative
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The product was not returned for investigation and the reported failure mode was not confirmed.The failure mode will be monitored for future reoccurrence.Alleged failure: after releasing finger from red suctioning button, it kept suctioning causing loss of insufflation.Probable root cause: manufacturing/assembly/ service error.Severe shipping conditions.Material/design error.Damaged equipment.User error.Board/ membrane failure.Damaged buttons.H3 other text : 81.
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Event Description
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It was reported that there was loss of insufflation during a case.
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Search Alerts/Recalls
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