Trinity with XL Heads E321.332Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055196937123), received between Mar 31, 2026 and Mar 31, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K130343); 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 31, 2026Insufficient Device Problem Information

  TRINITY REVISION OF THE ECIMA LINER AND METAL HEAD AFTER APPROXIMATELY 2 YEARS 2 MONTHS AND 2 WEEKS DUE TO DISLOCATION.

  Patient problems: Joint Dislocation

  MAUDE report 24739617 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K130343. One submission often covers many models, so check the product and lot details in each record.

• Z-1290-2021 · Jan 25, 2021 · Terminated
  Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis).
• Z-1291-2021 · Jan 25, 2021 · Terminated
  Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis).