Trinity Acetabular Hip System 321.03.536Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055343893227), received between Jul 9, 2026 and Sep 17, 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. How this data works · Data updated Oct 13, 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.

• InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem

  Trinity Dual Mobility revision (with OPS used at primary) of the CoCr Liner, ECiMa Insert and BIOLOX Delta Ceramic Head after approximately 1 year and 1 month as the patient was impinging.

  Patient problems: Joint Impingement

  MAUDE report 50803862 ↗
• InjuryJul 9, 2026Adverse Event Without Identified Device or Use Problem

  TRINITY DUAL MOBILITY (OPS USED IN PRIMARY) REVISION OF THE COCR LINER, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 YEAR AND 11 MONTHS DUE TO INFECTION WITH SUSPICION OF METALLOSIS. NOTE: LATE REPORT DUE TO THE REPORTER INFORMING VIGILANCE LATE. REPORTER MADE AWARE ON (B)(6) 2026 BUT DID NOT SUBMIT TO VIGILANCE UNTIL (B)(6) 2026.

  Patient problems: Unspecified Infection

  MAUDE report 25764003 ↗

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