(b)(4).Concomitant medical products: catalog number:00620205422 lot number:62601628 brand name: tm modular cup, catalog number:00625006530 lot number:62619020 brand name: bone screw, catalog number: 00625006520 lot number:62619022 brand name: bone screw, catalog number: 00625006520 lot number:62619022 brand name: bone screw, catalog number: 00631005032 lot number:62595137 brand name: xlpe liners, catalog number: 00771100900 lot number:61356526 brand name: m/l taper stem, catalog number: 00877703202 lot number:2702048 brand name: biolox head.Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2019-02553, 0002648920-2019-00433, 0002648920-2019-00435.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Device not returned for evalution.
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This follow-up report is being submitted to relay additional information.Medical records were provided and reviewed by a health care professional.Review of the available records identified that the patient was revised due to grossly loose acetabular components and scar-like changes on the trunnion.Upon entering the fascia, there was a large collection of fluid that was clear and looked like a synovial fluid.No greyness was evident to suggest some sort of metal issue based on the fluid alone.Large psuedocapsule present that was thick likely from the first revision.Trunnion was noted to have a fair amount of scarring.Not much in the way of corrosive changes or the black changes that are common with frank metallosis.No grossly evident corrosive changes in the femoral head.Synovitis was removed.The acetabular cup had migrated and overall version was well into the 60s.The cup was easily removed.There was some posterior-superior defect.Due to the loosening of the cup, there was a fairly-large acetabulum.Periprosthetic heterotopic ossification and osteophytic change at the greater trochanter appear unchanged.Blood loss of 1000cc is noted during the revision.Reported event was confirmed by review of medical records provided.Device history record was reviewed and no discrepancies were found.Root cause was unable to be determined.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.Device not returned for evaluation.
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