Trinity Acetabular Hip System with ECiMa Liners 322.04.936Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055343869871), received between Nov 12, 2025 and Aug 26, 2026 — classified as 2 injuries.

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.

• InjuryAug 26, 2026Adverse Event Without Identified Device or Use Problem

  TaperFit / Trinity revision of all components after nearly 8 months due to infection.

  Patient problems: Unspecified Infection

  MAUDE report 50447777 ↗
• InjuryNov 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY REVISION OF THE ECIMA LINER AND MODULAR HEAD AFTER NEARLY 4 WEEKS DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 23530539 ↗

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