Catalog Number 32810503000 |
Device Problem
Break (1069)
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Patient Problem
No Information (3190)
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Event Type
Injury
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Manufacturer Narrative
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(b)(4).This report will be amended when our investigation is complete.
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Event Description
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It is reported that the implant hinge pin has broken.
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Manufacturer Narrative
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Operative notes and x-rays were requested however none provided.The devices remain implanted therefore no devices or photos were provided.As such a determination on the condition of the devices could not be made.Review of the device history records did not find any deviations or anomalies.The devices were used for treatment.No other complaints of any type have been reported for the replacement kit or humeral assembly.With the provided information an exact cause could not be determined.
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Search Alerts/Recalls
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