Catalog Number 6001-088-227 |
Device Problem
Bent (1059)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 11/21/2016 |
Event Type
malfunction
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Event Description
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It was reported that the tip of the device was identified to be bent at the user facility.Although requested, the user facility was unable to provide any additional information regarding the event.
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Manufacturer Narrative
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The reported event that the unit was bent during an unknown time was confirmed through the device inspection.During functional inspection it was observed that the tip of the suction tube was deformed.The tube of the device is delicate and are susceptible to bending due to the small diameter of the tube and should be handled with special care.Any impact will cause product damage or operational failure due to battery movement.
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Event Description
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It was reported that the tip of the device was identified to be bent at the user facility.Although requested, the user facility was unable to provide any additional information regarding the event.
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Search Alerts/Recalls
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