The reported event that could be confirmed, based on available medical record and health care professionals.The device inspection was not possible as the product was not returned for investigation.The device history record could not be reviewed because the affected device was not returned, and the lot number was not communicated.A review of the labeling did not indicate any abnormalities.Upon further investigation of the ct scans by healthcare professionals the following was observed: after reviewing hcp opinion and surgeon¿s feedback we can conclude that tibial and talar component are well fixed.Pe also looks intact.However, stiffness and pain are the main cause of revision.Based on investigation, the root cause was attributed to a patient related issue.The failure is detected by stiffness and pain of tar.If the device is returned or any further information is provided, the investigation report will be reassessed.
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