Trinity Acetabular Hip System with ECiMa Liners 322.03.636Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 05055343869550), received between Jun 2, 2025 and Jul 29, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

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 18, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryJul 29, 2026Adverse Event Without Identified Device or Use Problem

  Trinity revision (OPS used in primary) of the ECiMa Liner after approximately 1 year and 9 months due to dislocation.

  Patient problems: Joint Dislocation

  MAUDE report 50070008 ↗
• InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 MONTH DUE TO DISLOCATION.

  Patient problems: Joint Dislocation

  MAUDE report 24000847 ↗
• InjurySep 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY REVISION AFTER APPROXIMATIVELY 6 WEEKS DUE TO INFECTION (WASHOUT ONLY, HEAD AND LINER NOT EXPLANTED AS SUPERFICIAL INFECTION).

  Patient problems: Unspecified Infection

  MAUDE report 23153584 ↗
• InjuryJul 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD DUE TO LINER DISASSOCIATING FROM THE SHELL.

  Patient problems: Joint Dislocation

  MAUDE report 22565603 ↗
• InjuryJun 6, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 2 MONTHS DUE TO PAIN AND IRRITATION.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 22156353 ↗
• InjuryJun 2, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 2 MONTHS AND 3 WEEKS DUE TO A POSSIBLE INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 22126223 ↗

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