Trinity Acetabular Hip System 325.04.042Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055343893531), received between Dec 22, 2025 and Feb 3, 2026 — classified as 2 injuries.

1 other recall cover devices cleared under the same FDA submission (K170359); 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.

• InjuryFeb 3, 2026Adverse Event Without Identified Device or Use Problem

  TRINITY REVISION AFTER APPROXIMATIVELY 3 MONTHS DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 24246246 ↗
• InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY DUAL MOBILITY REVISION OF THE COCR LINER, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 MONTH DUE TO PAIN, INFLAMMATION AND INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 23862892 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K170359. One submission often covers many models, so check the product and lot details in each record.

• Z-2608-2021 · Jul 28, 2021 · Terminated
  Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Dual Mobility, Size 4 42 insert/28 head, REF 325.04.042, Sterile; both are compone