Catalog Number 0620040690 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 11/13/2018 |
Event Type
malfunction
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Manufacturer Narrative
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The device manufacture date is not known at this time.However, should it become available it will be provided in future reports.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 surgery due to insufflation tubing disconnecting.
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Manufacturer Narrative
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Alleged failure: tubing disconnection.Probable root cause: use error.System design.Unwanted movement of internal components / wiring.Tubeset/gas supply inadvertently detached/loose.The product was not returned for investigation therefore the reported failure mode was not confirmed.The reported failure mode will be monitored for future reoccurrence.The device manufacturer date is not known.
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Event Description
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It was reported that there was loss of insufflation during surgery due to insufflation tubing disconnecting.
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Search Alerts/Recalls
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