No device associated with this report was received for examination.A complaint database search found one previous incident for the agility lp tibial sz2 rt.Review of the device history records did not reveal any related manufacturing deviations or anomalies on the provided product and lot code.The investigation could not draw any conclusions regarding the reported event.Based on the inability to determine a root cause, the need for corrective action was not indicated.Depuy considers the investigation closed at this time.Should the additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.
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