Catalog Number 6002-350-000 |
Device Problem
Bent (1059)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/22/2017 |
Event Type
malfunction
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Event Description
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It was reported that the tip of the device was found to be bent during a surgical procedure.No adverse consequences or procedural delays were reported with this event.
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Manufacturer Narrative
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The reported event was confirmed through the visual inspection.Any physical impact to the device can cause the reported event.
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Event Description
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It was reported that the tip of the device was found to be bent during a surgical procedure.No adverse consequences or procedural delays were reported with this event.
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Search Alerts/Recalls
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