Trinity Acetabular Hip System 321.03.352Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 05055196927476), received between Oct 10, 2025 and Jun 18, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Loss of Osseointegration” (1 report).

1 other recall cover devices cleared under the same FDA submission (K093472); 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJun 18, 2026Mechanical Problem

  TRINITY/TRINITY DUAL MOBILITY REVISION OF THE CLUSTER SHELL, BIOLOX DELTA CERAMIC MODULAR HEAD AND ECIMA INSERT AFTER APPROXIMATIVELY 3 YEARS AND 2 MONTHS DUE TO IMPINGEMENT.

  Patient problems: Joint Impingement

  MAUDE report 25545029 ↗
• InjuryFeb 4, 2026Loss of Osseointegration

  TRINITY REVISION OF CUP, ECIMA LINER, BIOLOX DELTA MOD HEAD AND SCREW AFTER 2 MONTHS DUE TO CUP SUBSIDING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24258454 ↗
• InjuryNov 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY DUAL MOBILITY REVISION OF THE CUP, SCREW, COCR LINER, ECIMA INSERT AND MODULAR HEAD AFTER APPROXIMATELY 2 YEARS DUE TO CUP LOOSENING AND IMPINGEMENT.

  Patient problems: Joint Laxity

  MAUDE report 23451609 ↗
• InjuryOct 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY AND METAFIX REVISION OF ALL PARTS AFTER APPROXIMATIVELY 1 MONTH DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 23265272 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K093472. One submission often covers many models, so check the product and lot details in each record.

• Z-2604-2021 · Jul 28, 2021 · Terminated
  Corin Trinity Screw, diameter 6.5mm 35mm Length, Cancellous Bone Screw, REF 321.035, Sterile; and Corin Trinity Screw, diameter 6.5mm 50mm Length, Cancellous Bone Screw, REF 321.05