Versafitcup CC TRIO Acetabular System 01.26.45.1148Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07630030807879), received between Nov 23, 2017 and May 8, 2026 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Issue” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMay 8, 2026Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY AFTER 2 YEARS AND 9 MONTHS DUE TO PAIN. THE SURGEON REVISED THE CUP, HEAD, AND LINER. THE SURGERY WAS SUCCESSFULLY COMPLETED.

  Patient problems: Implant Pain

  MAUDE report 25123176 ↗
• InjuryDec 11, 2020Loss of Osseointegration; Loss of Osseointegration

  REVISION SURGERY 6 YEARS AND 10 MONTHS AFTER PRIMARY SURGERY FOR CUP LOOSENING. ACETABULAR IMPLANTS REVISED SUCCESSFULLY.

  Patient problems: Joint Laxity

  MAUDE report 10991278 ↗
• InjuryNov 23, 2017Device Issue; Device Issue

  THE PE INLAY DID NOT WANT TO FIT WHEN INSERTING INTO THE CUP. THIS WAS ACHIEVED EVEN AFTER SEVERAL TESTS OF THE CUP AND THE INLAY FOR FOREIGN BODIES OR SIMILAR. A NEW INLAY WITH THE SAME SIZE WAS USED, WHICH WAS THEN PROPERLY FIT IN THE CUP. THE SURGERY COULD THEN BE SUCCESSFULLY TERMINATED WITHOUT PROBLEMS. THE CUP WAS NOT EXCHANGED.

  Patient problems: No Code Available

  MAUDE report 7057107 ↗