Catalog Number 6002-050-000 |
Device Problem
Deformation Due to Compressive Stress (2889)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 11/14/2017 |
Event Type
malfunction
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Event Description
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It was reported that handle and rotational adapter of the device were merged together after being hammered by the surgeon during use.The procedure was completed without clinically significant delay or adverse consequences, there was no known patient impact.
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Manufacturer Narrative
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Device evaluation: follow-up report submitted to document device evaluation results.
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Event Description
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It was reported that handle and rotational adapter of the device were merged together after being hammered by the surgeon during use.The procedure was completed without clinically significant delay or adverse consequences, there was no known patient impact.
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Search Alerts/Recalls
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