An event regarding revision of an unknown trident shell due to pain was reported.The event was confirmed through the medical records provided.Method and results: device evaluation and results: not performed as product was not returned.Medical records received and evaluation: review of these records confirms a revision of the patients left tha occurred in 2008 for iliopsoas tendinitis following a motor vehicle accident.No loosening or mechanical complication related to the implants was identified.The root cause of these complaints and revision tha cannot be determined as insufficient information was available.Device history review: could not be performed as lot code information was not provided.Complaint history review: could not be performed as lot code information was not provided.Conclusion: review of the medical records provided confirm a revision of the patients left tha occurred in 2008 for iliopsoas tendinitis following a motor vehicle accident.No loosening or mechanical complication related to the implants was identified.The root cause of these complaint and revision tha cannot be determined as insufficient information was available.The exact cause of the event could not be determined because insufficient information was provided.Additional information, including operative reports, surgical implant records from the 2018 revision surgery, dated pre and post op x-rays/ imaging from the index and revision surgeries and implant retrieval are needed to fully investigate the event.If further information becomes available or the product is returned, this investigation will be re-opened.Device not returned.
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