Versafitcup CC TRIO Acetabular System 01.26.45.1154Recalls & reported problems
Medacta International SA · Versafitcup Metalback CC Trio No-hole Ø54 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
- 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 07630030807909), received between Sep 8, 2017 and Jul 26, 2023 — classified as 5 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 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.
Most reported problems
Device problems
- Loose or Intermittent Connection3
- Appropriate Device Problem Term/Code Not Available2
- Osseointegration Problem1
Patient problems
- Hip Fracture1
- Inadequate Osseointegration1
- Joint Dislocation1
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Infection1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJul 26, 2023Osseointegration Problem; Osseointegration Problem
AT ABOUT 4 MONTHS AFTER THE PRIMARY, REVISION SURGERY DUE TO CUP MOBILIZATION IDENTIFIED ON POST-OPERATIVE X-RAYS. THE SURGEON REMOVED THE CUP, REAMED UP, IMPLANTED SUCCESSFULLY A SIZE BIGGER VERSAFITCUP CC TRIO CUP AND SECURED IT WITH 1 SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17396540 ↗InjurySep 15, 2021Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
5 YEARS AND 9 MONTHS AFTER THE PRIMARY SURGERY THE PATIENT CAME IN DUE TO A LOOSE CUP AND THE CAUSE OF THE LOOSE CUP IS UNKNOWN. THE SURGEON REVISED THE CUP AND LINER.
Patient problems: Inadequate Osseointegration
MAUDE report 12473172 ↗InjuryDec 18, 2019Loose or Intermittent Connection
5 DAYS POST-OP PATIENT PRESENTED WITH ACETABULAR FRACTURE OF THE MEDIAL WALL CAUSING THE CUP LOOSENING. ALL IMPLANTS WERE REVISED. THERE IS NO DEFINITIVE REASON FOR THE FRACTURE.
Patient problems: Hip Fracture
MAUDE report 9489460 ↗InjuryMar 6, 2019Loose or Intermittent Connection
REVISION SURGERY PERFORMED 1 YEAR AND 8 MONTHS AFTER PRIMARY DUE TO CUP AND STEM LOOSENING CAUSED BY INFECTION, PROPIONIBACTERIUM AVIDUM.
Patient problems: Unspecified Infection
MAUDE report 8394838 ↗InjurySep 8, 2017Appropriate Device Problem Term/Code Not Available
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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