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GLOBAL ICON 2240-10-060Recalls & reported problems

Depuy (Ireland) · GLOBAL ICON Stemless Shoulder System RESECTION GUIDE Size 11 · Class 2

All models of GLOBAL ICON (20)

Data updated Oct 18, 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 10603295420972), received between May 1, 2019 and May 1, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 18, 2026.

Most reported problems

Device problems

  • Material Twisted/Bent1

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.

  • MalfunctionMay 1, 2019Material Twisted/Bent; Material Twisted/Bent

    MDR NOTICED INSTRUMENT WAS BENT AND NEEDS TO BE REPLACED. NOTHING FELL INTO PATIENT. NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY . PATIENT STATUS/ OUTCOME / CONSEQUENCES --> NO.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8568904 ↗

Other Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained devices

All Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page