Trinity Acetabular Hip System with ECiMa Liners 322.02.932Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055343869833), received between Aug 7, 2026 and Aug 7, 2026 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryAug 7, 2026Adverse Event Without Identified Device or Use Problem

  Trinity revision (OPS used in primary) of ECiMa Liner after approx. 5 months due to dislocation.

  Patient problems: Joint Dislocation

  MAUDE report 50171412 ↗

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