Corin Metafix Hip Stem 579.0004Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055196900721), received between Dec 17, 2025 and Dec 17, 2025 — classified as 1 injury.

2 other recalls cover devices cleared under the same FDA submission (K082525); 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.

• InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT SUSTAINED A PERI-PROSTHETIC FRACTURE FOLLOWING A FALL AND REQUIRED METAFIX / TRINITY REVISION OF THE STEM, ECIMA LINER AND MOD HEAD AFTER APPROXIMATELY 5 YEARS AND 8 MONTHS.

  Patient problems: Bone Fracture(s)

  MAUDE report 23825543 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082525. One submission often covers many models, so check the product and lot details in each record.

• Z-1509-2022 · Jul 22, 2022 · Open, Classified
  Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
• Z-2609-2021 · Jul 28, 2021 · Terminated
  Corin MetaFix Hip Stem, Size 1, Short Neck, 135 degrees, Collared Hip Stem, REF 579.0201, Sterile.