MAUDE Adverse Event Report: CORIN LTD TRINITY; BIOLOX DELTA FEMORAL HEAD

Model Number	104.3605
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Joint Dislocation (2374)
Date of Event	02/09/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Per (b)(4) initial report.Additional information including: - post primary and pre revision x-rays.- operative notes (primary and revision) - patient weight, activity level and medical history - did the patient follow correct post-op protocol? - what was the patient doing at the time of the dislocations? - did the patient experience any slips / falls or other trauma post primary surgery? - an update on the patient post revision.Has been requested in order to progress with the investigation of this event and if received, will be provided in a supplemental report upon completion of the investigation the appropriate device details have been provided and the relevant device manufacturing records will be identified and reviewed.Please note: this report is filed with the fda due to an adverse event experienced with a device that is similar to those placed on the market in the usa, however, this event occured outside of the usa.The submission of this report does not constitute an admission that the device, reporting entity, entity's representative or distributor caused or contributed to this event.
Event or Problem Description
Trinity-i plus revision of the cup, screw, ecima liner and biolox delta ceramic head after approximately 1 year, 10 months and 2 weeks due to dislocation.
Event or Problem Description
Trinity-i plus revision of the cup, screw, ecima liner and biolox delta ceramic head after approximately 1 year, 10 months and 2 weeks due to dislocation.
Additional Manufacturer Narrative
Per (b)(4) final report.Please note: 6b was amended as it was identified that the correct date of primary surgery was(b)(6) 2024.Additional information including: post primary and pre revision x-rays.Operative notes (primary and revision).Patient weight, activity level and medical history.Did the patient follow correct post-op protocol? what was the patient doing at the time of the dislocations? did the patient experience any slips / falls or other trauma post primary surgery? an update on the patient post revision.Was requested in order to progress with the investigation of this event, however none of this information was provided and thus the scope of the investigation was limited.The appropriate device details were provided and the relevant device manufacturing records have been identified and reviewed.All final parts associated with these records conformed to material and dimensional specification at the time of manufacture.Based on the available information, no further investigation can be conducted and the root cause of the reported dislocation could not be determined.Therefore, this case is now considered closed, however, should any additional information be provided then this case may be re-opened for further investigation.Please note: this report is filed with the fda due to an adverse event experienced with a device that is similar to those placed on the market in the usa, however, this event occured outside of the usa.The submission of this report does not constitute an admission that the device, reporting entity, entity's representative or distributor caused or contributed to this event.

• Brand Name: TRINITY
• Common Device Name: BIOLOX DELTA FEMORAL HEAD
• Manufacturer (Section D): CORIN LTD; the corinium centre; cirencester, gloucestershire GL7 1 YJ; UK GL7 1YJ
• Manufacturer (Section G): CORIN LTD; the corinium centre; cirencester, gloucestershire GL7 1 YJ; UK GL7 1YJ
• Manufacturer Contact: franck didier ; the corinium centre; cirencester, gloucestershire GL7 1-YJ ; UK GL7 1YJ
• MDR Report Key: 24505462
• Report Number: 9614209-2026-00035
• Device Sequence Number: 21322206
• Product Code: LZO
• UDI-Device Identifier: 05055343898116
• UDI-Public: 05055343898116
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K110087
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/29/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 104.3605
• Device Catalogue Number: N/A
• Device Lot Number: 551454
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/11/2026
• Supplement Date Received by Manufacturer: 02/11/2026
• Initial Report FDA Received Date: 03/04/2026
• Supplement Report FDA Received Date: 04/29/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/13/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: TRINITY LINER: 322.04.936, 550997; TRINITY LINER: 322.04.936, 550997; TRINITY SCREW: 321.035, 532264; TRINITY SCREW: 321.035, 532264; TRINITY-I PLUS SHELL: 324.04.754, 531088; TRINITY-I PLUS SHELL: 324.04.754, 531088
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 60 YR
• Patient Sex: Female