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GLOBAL ICON 1140-20-354Recalls & reported problems

Depuy (Ireland) · GLOBAL ICON STEMLESS SHOULDER SYSTEM HUMERAL HEAD DIAMETER 54mm +3 · Class 2 · Implant

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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295451624), received between Nov 25, 2020 and Nov 25, 2020 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Pain1
  • Unspecified Musculoskeletal problem1

Recent adverse event reports

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

  • InjuryNov 25, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE ROTATOR CUFF MAY HAVE BEEN DEFICIENT CAUSING PAIN. AFFECTED SIDE IS LEFT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Pain; Unspecified Musculoskeletal problem

    MAUDE report 10905253 ↗

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