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Model Number 6143.1001 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
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Event Date 09/30/2020 |
Event Type
Injury
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Manufacturer Narrative
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Investigation confirmed that there was no system malfunction found.The root cause was user technique.
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Event Description
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It was reported that a revision surgery was done to remove and replace 4 screws from t12 and l2 that were not placed to plan.
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Search Alerts/Recalls
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