Catalog Number 254500041 |
Device Problem
Insufficient Information (3190)
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Patient Problem
Injury (2348)
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Event Date 10/09/2017 |
Event Type
Injury
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Manufacturer Narrative
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Product complaint # = > (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Investigation summary = > the device associated with this report was not returned.The investigation could not verify or identify any product contribution to the reported event with the information provided as the reported device was not returned for evaluation.Based on the inability to determine a root cause, a need for corrective action is not indicated.
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Event Description
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It was reported that the long intramedullary distal femoral cutting guide exited the canal.
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Manufacturer Narrative
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Product complaint # = > pc(b)(4) investigation summary = > the device associated with this report was not returned.The investigation could not verify or identify any product contribution to the reported event with the information provided as the reported device was not returned for evaluation.Based on the inability to determine a root cause, a need for corrective action is not indicated.
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Manufacturer Narrative
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If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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