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CORAIL 3L92520Recalls & reported problems

Depuy (Ireland) · CORAIL HIP SYSTEM CEMENTLESS FEMORAL STEM 12/14 AMT 135 DEGREES KS SIZE 20 HA COATED STANDARD NO COLLAR · Class 2 · Implant

All models of CORAIL (121)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295168843), received between May 19, 2022 and May 19, 2022 — classified as 1 injury.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Swelling/ Edema1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryMay 19, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PATIENT WAS REVISED DUE TO SICKNESS AND SWOLLEN RIGHT THIGH. IT WAS DETERMINED THAT THE THIGH AND THE HIP JOINT WERE INFECTED. I&D WITH COMPONENT REMOVAL WAS PERFORMED. THE CUP AND LINER WERE STRYKER COMPONENTS (ALSO REMOVED). DOI: (B)(6) 2020; DOR: (B)(6) 2022; AFFECTED SIDE: RIGHT HIP.

    Patient problems: Swelling/ Edema; Unspecified Infection

    MAUDE report 14434140 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

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