Catalog Number 0620040690 |
Device Problem
Disconnection (1171)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 12/28/2018 |
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 the insufflation tubing disconnected during the procedure.
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Manufacturer Narrative
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The product was returned for investigation and the failure mode will be monitored for future reoccurrence.The reported failure mode was confirmed.Alleged failure: we were notified of a complaint from a customer stating that the insufflation tubing was disconnecting from the head of the device.The failure(s) identified in the investigation is consistent with the complaint record.The probable root cause could be manufacturing.The device manufacture date is not known.
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Event Description
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It was reported that the insufflation tubing disconnected during the procedure.
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Search Alerts/Recalls
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