Catalog Number 6001-022-000 |
Device Problem
Bent (1059)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 09/08/2016 |
Event Type
malfunction
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Event Description
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It was reported that during a surgical procedure the tip of the device was found to be bent.No adverse consequences or procedural delays were reported with this event.
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Manufacturer Narrative
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The reported event that the tip of the device was bent was confirmed through the device inspection.Any physical impact to the navigated instrument can cause product damage or operational failure due to battery movement.
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Event Description
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It was reported that during a surgical procedure the tip of the device was found to be bent.No adverse consequences or procedural delays were reported with this event.
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Search Alerts/Recalls
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