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GLOBAL 2236-80-080Recalls & reported problems

Depuy Orthopaedics, Inc. · GLOBAL ANCHOR PEG PERIPHERAL GUIDE · Class 1

All models of GLOBAL (20)

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 10603295106302), received between Sep 8, 2017 and Sep 8, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionSep 8, 2017Break; Break

    IT WAS REPORTED THAT THE SURGEON BROKE THE GOLD PERIPHERAL GLENOID WHILE TRYING TO TAKE IT OUT OF THE GLENOID. IT SPLIT INTO TWO PIECES. NOTHING WAS LEFT BEHIND IN THE PATIENT. THE GUIDE WAS BROKEN AFTER USING IT SO IT DID NOT HOLD UP SURGERY. IT IS BEING RETURNED TO CORPORATE.

    Patient problems: No Information

    MAUDE report 6851600 ↗

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Sources and updates

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