Skip to content

GLOBAL ICON 2240-11-042Recalls & reported problems

Depuy (Ireland) · GLOBAL ICON Stemless Shoulder System HUMERAL PREP GUIDE Size 42 · 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 10603295427049), received between Aug 24, 2023 and Aug 24, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

  • Device-Device Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 24, 2023Device-Device Incompatibility; Device-Device Incompatibility

    IT WAS REPORTED THAT THE PATIENT HAD A TOTAL SHOULDER. DURING HUMERAL PREPARATION THE PIN BOUND IN THE PREP PLATE. NO TIME DELAY. NO HARM, ALL PARTS IDENTIFIED. PIN NOW PASSES THROUGH PLATE WITH DIFFICULTY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17612719 ↗

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