EXACTECH, INC. NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTED OR NON-POROUS
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Catalog Number 130-36-52 |
Device Problem
Naturally Worn (2988)
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Patient Problem
Osteolysis (2377)
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Event Date 07/21/2023 |
Event Type
Injury
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Manufacturer Narrative
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H10.D10.Concomitants: 4142528 170-36-93 - biolox delta femoral head 36mm od, -3.5mm.4169648 180-01-52 - nv crown cup clstr hole 52mm group 2.3754797 180-65-35 - alteon 6.5mm screw, 35mm.4143375 188-01-08 - wedge plasma x/o sz 8.These devices are used for treatment and not in diagnosis.Pending investigation.
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Event Description
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It was reported via legal documentation that a patient had a right total hip arthroplasty on (b)(6) 2015, and then experienced revision surgical procedure on (b)(6) 2023 approximately 7 years and 7 months after initial implant.No images were provided.There is no other information available.
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Search Alerts/Recalls
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