Catalog Number 6000-011-000 |
Device Problem
Bent (1059)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/11/2013 |
Event Type
malfunction
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Event Description
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It was reported that the tip of the large pointer was bent during testing or set up at the user facility.There was no patient involvement and no adverse consequences associated with the device.
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Event Description
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It was reported that the tip of the large pointer was bent during testing or set up at the user facility.There was no patient involvement and no adverse consequences associated with the device.
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Manufacturer Narrative
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Device not yet returned for investigation.
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Manufacturer Narrative
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During failure analysis, the reported event that the pointer tip was bent was confirmed through the visual inspection and production software.During the device evaluation, we were unable to determine what caused the bent tip.It is possible rough or improper handling led to bent tip.The device was repaired and returned to stryker stock.
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Search Alerts/Recalls
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