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 06/23/2016 |
Event Type
malfunction
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Event Description
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It was reported that during a procedure conducted at the user facility the tip of the device was bent.No impact to the patient or procedural delays were reported with this event.
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Manufacturer Narrative
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The reported event that tip of the device was bent was confirmed through the visual inspection.It was observed that the tip is deformed.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 procedure conducted at the user facility the tip of the device was bent.No impact to the patient or procedural delays were reported with this event.
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Search Alerts/Recalls
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