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CORAIL L95680Recalls & reported problems

Depuy (Ireland) · CORAIL · Class 1

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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295261858), received between Jun 5, 2019 and Jun 5, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Material Deformation1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJun 5, 2019Material Deformation; Material Deformation

    DURING INSPECTION IN LOCAL DISTRIBUTION CENTER, IT WAS NOTICED THAT PRODUCT WAS DAMAGED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8670550 ↗

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Sources and updates

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