Versafitcup CC TRIO Acetabular System 01.26.3244STTRecalls & reported problems
Medacta International SA · Flat PE liner Ø 32 / E · 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
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07630030807589), received between Jan 14, 2021 and Mar 13, 2025 — classified as 5 injuries.
The most frequently reported specific device problem is “Naturally Worn” (4 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, 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
- Naturally Worn4
- Material Integrity Problem1
Patient problems
- Osteolysis3
- Failure of Implant1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryMar 13, 2025Naturally Worn; Naturally Worn
AT ABOUT 7 YEARS AND 5 MONTHS FROM PRIMARY THE SURGEON PERFORMED A REVISION DUE TO WEAR OF PE LINER. DISPLACEMENT OF HEAD CENTER OF ROTATION WAS REPORTED WHILE CUP FIXATION WAS GOOD. HEAD, LINER AND CUP WERE ALL REVISED AND SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21594646 ↗InjuryJul 15, 2022Naturally Worn
AT ABOUT 7 YEARS AFTER THE PRIMARY, THE PATIENT CAME IN REPORTING PAIN IN THE HIP. REVISION SURGERY WAS PERFORMED AND IT WAS DISCOVERED ECCENTRIC WEAR OF THE LINER WITH SUBSEQUENT OSTEOLYSIS.
Patient problems: Osteolysis
MAUDE report 15025736 ↗InjuryDec 22, 2021Material Integrity Problem; Material Integrity Problem
REVISION SURGERY AT 4 YEARS AND 9 MONTHS AFTER PRIMARY DUE TO OSTEOLYSIS THAT CAUSED THE STEM MOBILIZATION, LINER WEAR SUSPECTED BY THE SURGEON. STEM, HEAD AND LINER WERE REVISED.
Patient problems: Osteolysis
MAUDE report 13060041 ↗InjuryAug 23, 2021Naturally Worn
3 YEARS AND 11 MONTHS AFTER THE PRIMARY SURGERY, CUP, HEAD AND LINER WERE REVISED DUE TO SUSPECTED LINER WEAR. THE SURGEON IMPLANTED SIZE 54 HEAD, REINFORCEMENT CAGE WITH 3 SCREWS AND APRICOT 48 CUP.
Patient problems: Failure of Implant
MAUDE report 12352941 ↗InjuryJan 14, 2021Naturally Worn
WORN INLAY OF A VERSAFITCUP CC TRIO IMPLANTED ON 2014, OSTEOLYSIS IN THE FEMUR. REVISION PERFORMED ON (B)(6) 2020 (6 YEARS AND 2 MONTHS AFTER PRIMARY), LINER AND HEAD WERE REPLACED.
Patient problems: Osteolysis
MAUDE report 11169837 ↗
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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