Versafitcup CC TRIO Acetabular System 01.26.45.0062Recalls & reported problems
Medacta International SA · Versafitcup Metalback CC Trio Ø62 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 07630030807824), received between Sep 17, 2019 and Feb 26, 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
- Appropriate Device Problem Term/Code Not Available2
- Device Appears to Trigger Rejection1
- Device Dislodged or Dislocated1
- Positioning Problem1
Patient problems
- Joint Disorder1
- Medical device site infection1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 26, 2025Device Appears to Trigger Rejection; Device Appears to Trigger Rejection
REVISION SURGERY DUE TO INFECTION AT ABOUT 6 YEARS FROM PRIMARY. NO FURTHER INFO ARE AVAILABLE.
Patient problems: Medical device site infection
MAUDE report 21469482 ↗InjuryJul 23, 2020Device Dislodged or Dislocated; Positioning Problem; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY ON THE (B)(6) 2020 WITH REMOVING THE CUP, INLAY AND HEAD AFTER THE PATIENTS HIP DISLOCATED TWICE SINCE PRIMARY SURGERY ON THE (B)(6) 2020. AS REPORTED BY THE SURGEON, THE CUP WAS MALPOSITIONED WITH TOO MUCH INCLINATION. 6 MONTHS AFTER PRIMARY THE CUP WAS REMOVED AND REPLACED.
Patient problems: Joint Disorder
MAUDE report 10313461 ↗InjurySep 17, 2019Appropriate Device Problem Term/Code Not Available
PATIENT HAD AN INFECTED HIP. WE WERE INFORMED ON THE (B)(6) 2019 OF THE REVISION SURGERY PLANNED AND PERFORMED ON THE (B)(6) 2019, 11 MONTHS AFTER PRIMARY. ALL COMPONENTS HAVE BEEN REMOVED. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Unspecified Infection
MAUDE report 9075828 ↗
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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