Versafitcup CC TRIO Acetabular System 01.26.3248HCTRecalls & reported problems
Medacta International SA · Flat PE HC liner Ø 32 / F · 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 07630030807619), received between Sep 20, 2019 and May 25, 2022 — classified as 3 injuries.
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
- Appropriate Device Problem Term/Code Not Available2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection2
- Osteolysis1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMay 25, 2022Appropriate Device Problem Term/Code Not Available
DURING AN XRAYS CONTROL, IT WAS NOTICED THAT OSTEOLYSIS IS PRESENT AROUND THE STEM (GREATER TROCHANTER) AND THE HEAD IS NOT IN THE MIDDLE OF THE POLY LINER. STEM AND LINER WERE REVISED 7 YEARS AND 10 MONTHS AFTER PRIMARY.
Patient problems: Osteolysis
MAUDE report 14494536 ↗InjuryFeb 13, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY PERFORMED AFTER 3 YEARS AND 9 MONTHS FROM THE PRIMARY DUE TO AN INFECTION. THE SURGEON REVISED THE LINER.
Patient problems: Unspecified Infection
MAUDE report 9706056 ↗InjurySep 20, 2019Adverse Event Without Identified Device or Use Problem
ON THE (B)(4) 2019 WE WERE INFORMED OF A REVISION SURGERY PLANNED AND PERFORMED ON THE (B)(6) 2019. THE PATIENT HAD AN INFECTION. THE SURGEON DECIDED THAT THE INFECTION NEEDED TO BE WASHED OUT AND THE LINER AND HEAD NEEDED TO BE EXCHANGE 1 MONTH AND 1 DAY AFTER PRIMARY. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Unspecified Infection
MAUDE report 9096673 ↗
Other Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate devices
- Novation 130-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls156 reports
- Novation 130-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls79 reports
- CORAIL 3L92511Depuy (Ireland) · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate158 reports
- Acumatch A Series 138-36-29Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate3 recalls1 report
- Novation 136-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls43 reports
- Novation 130-32-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls33 reports
- Novation 132-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls26 reports
- Novation 136-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls22 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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