Trinity Acetabular Hip System with ECiMa Liners 322.03.932Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055343869840), received between May 20, 2025 and Mar 12, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (1 report).

1 other recall cover devices cleared under the same FDA submission (K111481); they may or may not involve this specific model.

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 16, 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.

• InjuryMar 12, 2026Fracture

  TRINITY REVISION OF THE CUP, ECIMA LINER, BIOLOX DELTA CERAMIC HEAD AND SCREW AFTER APPROXIMATELY 1 YEAR AND 6 MONTHS. THE ECIMA LINER WAS LOOSE AND HAD FRACTURED THROUGH THE POSTERIOR RIM AND EPW JUNCTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24579301 ↗
• InjuryMay 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY / TRIFIT TS REVISION OF ALL COMPONENTS AFTER APPROXIMATIVELY 3 YEARS AND 2 MONTHS DUE TO INFECTION. AN ANTIBIOTIC SPACER WAS USED DURING THE REVISION.

  Patient problems: Unspecified Infection

  MAUDE report 22053295 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K111481. One submission often covers many models, so check the product and lot details in each record.

• Z-2606-2021 · Jul 28, 2021 · Terminated
  Corin Trinity Liner ECIMA, diameter 40mm Neutral Offset, Taper Size 4, REF 322.04.640, Sterile; and Corin Trinity Liner ECIMA, diameter 36mm Neutral 4mm EPW, Taper Size 4 (Elevate