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Catalog Number 26-1221 |
Device Problem
Insufficient Information (3190)
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Patient Problem
No Code Available (3191)
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Event Date 03/24/2016 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).It has been communicated that the device and/or lot information is not available for evaluation.Without the device and/or lot information it is not possible for codman to conduct a proper investigation.If at some point the device and/or lot information does become available, this complaint will be re-opened, evaluated and a follow up report will be filed.Trends will be monitored for this and similar complaints.At the present time this complaint is considered closed.Device discarded.
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Event Description
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During perforating the skull, the device damaged the dura mater.Further information would be provided as soon as we receive it from the facility.On (b)(6) 2016 per affiliate, sample was discarded at the facility.
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Search Alerts/Recalls
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