Arcos Modular Revision Hip System 11-302015Recalls & reported problems
Biomet Orthopedics, LLC · Class 3 · Implant
All models of Arcos Modular Revision Hip System (71)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304468061), received between Aug 28, 2023 and Aug 28, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
Patient problems
- Failure of Implant1
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2023Fracture; Adverse Event Without Identified Device or Use Problem; Fracture; Adverse Event Without Identified Device or Use Problem
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 17630501 ↗
Other Prosthesis, hip, semi-constrained (metal cemented acetabular component) devices
- Omnifit 2001-2246Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained (metal cemented acetabular component)1 recall0 reports
- Taperloc Complete Micro Primary Femoral 51-107150Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)41 reports
- Taperloc Complete Micro Primary Femoral 51-107140Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)36 reports
- Dynasty DSBFGD52Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)12 reports
- CONSERVE® 38AM4600Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)8 reports
- CONSERVE® 38AM4804Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)7 reports
- CONSERVE® 38AM4404Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)6 reports
- TRANSCEND® 26000025Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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