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CORAIL L971109Recalls & reported problems

Depuy (Ireland) · CORAIL HIP SYSTEM CEMENTLESS FEMORAL STEM HA COATED 12/14 AMT 135 DEGREES HIGH OFFSET COLLAR SIZE 9 · Class 2 · Implant

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 10603295455288), received between Oct 19, 2020 and Oct 19, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (1 report).

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

Device problems

  • Loss of Osseointegration1

Patient problems

  • Inadequate Osseointegration1
  • No Code Available1
  • Pain1

Recent adverse event reports

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

  • InjuryOct 19, 2020Loss of Osseointegration; Loss of Osseointegration

    REVISION OF CORAIL STEM TO CORAIL REVISION ON (B)(6) 2020. CHANGE OF LINER, CHANGE HEAD. REVISION DUE TO PAIN AND JOINT INSTABILITY SECONDARY TO LOOSENING OF THE FEMORAL STEM. NO REPORTED SURGICAL DELAY OR PATIENT COMPLICATIONS.

    Patient problems: Inadequate Osseointegration; No Code Available; Pain

    MAUDE report 10698434 ↗

Other Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate devices

All Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.