Catalog Number 6002-700-000 |
Device Problem
Bent (1059)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/12/2013 |
Event Type
malfunction
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Event Description
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It was reported that the tip of the awl was bent during testing or setup prior to a procedure.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 awl was bent during testing or setup prior to a procedure.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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The reported event that the pointer tip was bent was duplicated; it was confirmed through visual inspection that the device had a bent tip.It is possible that bending forces caused the reported event.The pointer was repaired and put back into stryker stock.
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Search Alerts/Recalls
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