BI-MENTUM Cemented CupRecalls & reported problems across all models
Soc Etudes Recherches Fabrication · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 28
- Deaths reported
- 0
- Injuries reported
- 28
- Recalls
- 0
We found 8 models of BI-MENTUM Cemented Cup by Soc Etudes Recherches Fabrication in the FDA's device registry (GUDID). Together they are named in 28 adverse event reports in the FDA's MAUDE database, received between Aug 3, 2021 and Jan 9, 2026 — classified as 28 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported BI-MENTUM Cemented Cup problems
Device problems
- Adverse Event Without Identified Device or Use Problem23
- Device Dislodged or Dislocated3
- Insufficient Device Problem Information2
- Loss of Osseointegration2
- Loosening of Implant Not Related to Bone-Ingrowth1
- Patient Device Interaction Problem1
- Unstable1
Patient problems
- Pain11
- Joint Dislocation6
- Pelvic Pain4
- Inadequate Osseointegration3
- Insufficient Information3
- Joint Laxity3
- Unspecified Infection3
- Bone Fracture(s)2
BI-MENTUM Cemented Cup models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 51Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented8 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 47Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented6 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 49Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate3 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 55Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented3 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 57Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate3 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 43Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented2 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 59Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented2 reports
- BI-MENTUM Cemented Cup BI-MENTUM Cemented Cup 61Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate1 report
Recent BI-MENTUM Cemented Cup adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJan 9, 2026Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem
PATIENT OCCURED A REVISION DUE TO DISLOCATION AND PAIN.
Patient problems: Joint Dislocation; Pain
MAUDE report 24017542 ↗InjuryDec 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
(B)(6) FIRST REPORT OF RETRIEVALS FOR STATEMENT OF WORK FOR Q4 OF 2025. (B)(6) IS THE RESEARCH LOCATION, AND NOT THE FACILITY OF PLACEMENT. A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS. REASON FOR REVISION: REVISION FOR DISLOCATION AND PAIN. THE REVISED CERAMIC HEAD SHOWS MODERATE METAL TRANSFER.
Patient problems: Joint Dislocation; Pain
MAUDE report 23933968 ↗InjuryDec 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT OCCURED A CUP REVISION ON THE RIGHT HIP DUE TO PAIN.
Patient problems: Pelvic Pain
MAUDE report 23726384 ↗InjuryNov 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO PAIN. DOI- UNKNOWN. DOR- (B)(6) 2025. AFFECTED SIDE- RIGHT HIP.
Patient problems: Pain
MAUDE report 23606221 ↗InjuryOct 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT OCCURED A REVISION DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23301345 ↗InjuryOct 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjurySep 23, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
InjurySep 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO PAIN. DOI: UNKNOWN DOR: (B)(6) 2025 AFFECTED SIDE: RIGHT HIP.
Patient problems: Pain
MAUDE report 23030719 ↗InjurySep 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE BIMENTUM CEMENTED CUP DISLODGED FROM PATIENT'S SOCKET. THERE WAS LOOSENING OF THE BIMENTUM CEMENTED CUP AT CEMENT/IMPLANT INTERFACE. CEMENT MANUFACTURER WAS UNKNOWN. DOI: UNKNOWN. DOR:(B)(6), 2025. AFFECTED SIDE: RIGHT HIP.
Patient problems: Insufficient Information
MAUDE report 23014960 ↗InjuryAug 27, 2025Loss of Osseointegration; Loss of Osseointegration
BIMENTUM CEMENTED CUP DISLODGED FROM PATIENT'S SOCKET. PATIENT OCCURED A LOOSENING OF THE BI-MENTUM CEMENTED CUP AT CEMENT / IMPLANT INTERFACE. CEMENT MANUFACTURER IS UNKNOWN. AFFECTED SIDE: RIGHT HIP.
Patient problems: Inadequate Osseointegration
MAUDE report 22904603 ↗InjuryAug 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT OCCURED A REVISION OF A BI-MENTUM CEMENTED CUP DUE TO PAIN.
Patient problems: Pelvic Pain
MAUDE report 22891167 ↗InjuryAug 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT OCCURED A REVISION OF THE BI-MENTUM CEMENTED CUP DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 22891159 ↗InjuryAug 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT REVISED DUE TO PAIN. AFFECTED SIDE: RIGHT HIP.
Patient problems: Pain
MAUDE report 22804289 ↗InjuryJul 31, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
PATIENT OCCCURED A LOOSENING AT UNKNOWN INTERFACE.
Patient problems: Inadequate Osseointegration
MAUDE report 22680524 ↗InjuryMar 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
UPON FURTHER REVIEW, THE PREVIOUSLY REPORTED EVENT WAS DETERMINED TO HAVE OCCURRED IN NEW ZEALAND AND THEREFORE DOES NOT MEETING REPORTING REQUIREMENTS AS AN IMPORTER. THIS DOES NOT MEET THE DEFINITION OF A COMPLAINT AND THEREFORE PLEASE DISREGARD ANY FURTHER REPORTS ON 1818910-2025-150001.
Patient problems: Joint Dislocation; Joint Laxity; Unspecified Tissue Injury
MAUDE report 21696083 ↗
Other Soc Etudes Recherches Fabrication products
All Soc Etudes Recherches Fabrication devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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