MAUDE Adverse Event Report: S.E.R.F Societe dEtudes Recherche Fabrication BI-MENTUM PE liner 28/57; Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous

Catalog Number	DS10015728
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Date of Event	07/27/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
No new information available.
Event or Problem Description
The patient reported pain and was revised.
Additional Manufacturer Narrative
Reported event: an event regarding pain involving bi-mentum pe liner 28/57 was reported.The event was not confirmed.Method & results: device evaluation and results: not performed as product was not returned.Clinician review: no medical records were received for review with a clinical consultant.Device history review: all devices were manufactured and accepted into final stock with no relevant reported discrepancies.Complaint history review: there have been no other similar events for the reported lot.Conclusion: the exact cause of the event could not be determined because insufficient information was provided.Additional information including operative reports, progress notes, x-rays and return of the device are needed to fully investigate the event.If further information becomes available or the product is returned, this investigation will be re-opened.Product surveillance will continue to monitor for trends.Corrective action/preventive action: no action is required at this time as there is no indication to suggest a product non-conformity or unanticipated hazard.
Additional Manufacturer Narrative
An evaluation of the device cannot be performed as the device was not returned to the manufacturer.Should additional information become available it will be reported in a supplemental report upon completion of the investigation.

• Brand Name: BI-MENTUM PE liner 28/57
• Common Device Name: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous
• Manufacturer (Section D): S.E.R.F Societe dEtudes Recherche Fabrication; 85 avenue des bruyeres; 69150 decines-charpieu; decines 69150 ; FR 69150
• Manufacturer (Section G): S.E.R.F Societe dEtudes Recherche Fabrication; 85 avenue des bruyeres; 69150 decines-charpieu; decines 69150 ; FR 69150
• Manufacturer Contact: margaux baboulaz ; 85 avenue des bruyeres; 69150 decines-charpieu; decines 69150 ; FR 69150 ; +33()472056010
• MDR Report Key: 50171601
• Report Number: 3008668801-2026-00024
• Device Sequence Number: 9860165
• Product Code: LZO
• UDI-Device Identifier: 03662200015696
• UDI-Public: 03662200015696
• Combination Product (Y/N): N
• Initial Reporter State: SC
• Initial Reporter Country: US
• PMA/510(K) Number: K181744
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 08/17/2026

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 Expiration Date: 10/31/2024
• Device Catalogue Number: DS10015728
• Device Lot Number: 1909327A
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 07/30/2026
• Supplement Date Received by Manufacturer: 08/11/2026
• Initial Report FDA Received Date: 08/07/2026
• Supplement Report FDA Received Date: 08/17/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Sex: Unknown