Versafitcup CC TRIO Acetabular System 01.26.3248HCATRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630030807602), received between Apr 29, 2020 and May 24, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 24, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT UNDERGONE A PRIMARY SURGERY ON THE (B)(6) 2015. ON THE (B)(6) 2018, THE PATIENT CAME IN REPORTING SQUEAKING IN THE HIP JOINT. THE SURGEON REVISED SUCCESSFULLY THE CERAMIC LINER AND BALL HEAD AND REPLACED THEM WITH A HOODED PE HC LINER Ø 32 / F, HEAD BIOLOX Ø32 AND A SLEEVE SIZE L. ON THE (B)(6) 2024, THE PATIENT HAS BEEN REVISED DUE TO MULTIPLE DISLOCATIONS AND IT IS UNKNOWN HOW THEY HAVE BEEN TREATED. VERSAFITCUP AND LINER HAVE BEEN REVISED WITH COMPETITOR DEVICES, WHILE THE CERAMIC BALL HEAD AND SLEEVE HAVE BEEN REVISED WITH A MEDACTA 28MM COCR HEAD.

  Patient problems: Joint Dislocation

  MAUDE report 19390102 ↗
• InjuryApr 29, 2020Appropriate Device Problem Term/Code Not Available

  THE PATIENT HAD BEEN COMPLAINING OF INSTABILITY AFTER AN INCIDENT OF BENDING OVER AND LIFTING SOMETHING. THE SURGEON THEN REVISED HEAD AND LINER (8 YEARS AND 7 MONTHS AFTER PRIMARY SURGERY) IN ORDER TO IMPLANT A DUAL MOBILITY SYSTEM.

  Patient problems: Joint Disorder

  MAUDE report 10008594 ↗