Versafitcup CC TRIO Acetabular System 01.26.45.0060Recalls & reported problems
Medacta International SA · Versafitcup Metalback CC Trio Ø60 mm · Class 2 · Implant
All models of Versafitcup CC TRIO Acetabular System (32)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07630030807817), received between Oct 26, 2017 and Jul 1, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Appears to Trigger Rejection” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device Appears to Trigger Rejection1
- Loose or Intermittent Connection1
- Unstable1
Patient problems
- Joint Disorder1
- Metal Related Pathology1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WITH OCCASIONAL PAIN, X-RAYS SHOWED NO ISSUE. SOME TIME LATER, THE PATIENT PRESENTS WITH LUMBAR PAIN. CT SCAN PERFORMED: THE RADIOLOGIST ENLARGED THE FIELD AND FOCUSED ON THE LOWER PELVIS, REVEALING AN AREA OF PERIPROSTHETIC METALLOSIS. PUNCTURE WAS NEGATIVE, NO INFECTION, BUT BLACKISH LIQUID WAS PRESENT. ABOUT 9 YEARS AND 10 MONTHS AFTER THE PRIMARY SURGERY, THE SURGEON CLEANED THE JOINT AND CHANGED THE INSERT AND THE FEMORAL HEAD. STEM AND CUP LEFT IN SITU.
Patient problems: Metal Related Pathology
MAUDE report 22369344 ↗InjuryJul 10, 2024Device Appears to Trigger Rejection; Device Appears to Trigger Rejection
HIP REVISION FOR INFECTION. AT ABOUT 1 YEAR AND 7 MONTHS FORM PRIMARY ALL IMPLANTS WERE REVISED.
Patient problems: Unspecified Infection
MAUDE report 19711167 ↗InjuryOct 26, 2017Loose or Intermittent Connection; Unstable
THE PATIENT CAME IN COMPLAINING OF INSTABILITY. THE SURGEON DETERMINED THE CUP WAS LOOSE. THE SURGEON BELIEVES THE CAUSE MAY BE FROM THE ACETABULAR REAMING IN THE PRIMARY SURGERY. THE SURGEON PLANNED TO REVISE THE CUP AND LINER. THE SURGEON REVISED THE HEAD, LINER AND CUP. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Joint Disorder
MAUDE report 6979321 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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