Trinity Acetabular Hip System 325.03.040Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 05055343893524), received between Jul 11, 2025 and Sep 22, 2026 — classified as 4 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem

  Trinity Dual Mobility and Paragon revision (with OPS used in primary surgery) of all devices after approximatively 3 weeks due to infection.Note: the Paragon stem GM08001-203-03 is not cleared in the USA.

  Patient problems: Unspecified Infection

  MAUDE report 50851396 ↗
• InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem

  Trinity Dual Mobility revision of the Cup, CoCr Liner and ECiMa Insert after approximately 1 month due to infection.Please note: this is the 2nd revision for this patient. A previous revision was performed and reported under reference 9614209-2025-00635.

  Patient problems: Unspecified Infection

  MAUDE report 50753891 ↗
• InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY DUAL MOBILITY REVISION OF THE ECIMA INSERT AND COCR LINER AFTER APPROXIMATELY 2 YEARS AND 4 MONTHS DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 23861713 ↗
• InjuryJul 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  TRINITY BIOLOX DELTA REVISION AFTER APPROXIMATIVELY 3 WEEKS DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 22477449 ↗

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