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GLOBAL ADVANTAGE 2128-61-001Recalls & reported problems

Depuy Orthopaedics, Inc. · GLOBAL ADVANTAGE GLENOID REAMER 44mm · Class 1

All models of GLOBAL ADVANTAGE (47)

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 10603295089230), received between Oct 4, 2019 and Oct 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Dull, Blunt” (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

  • Dull, Blunt1

Patient problems

  • Not Applicable1

Recent adverse event reports

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

  • MalfunctionOct 4, 2019Dull, Blunt; Dull, Blunt

    IT WAS REPORTED THAT THIS WAS AN ENTIRE ARTIFICIAL JOINT REPLACEMENT PROCEDURE TREATING SHOULDER JOINT OSTEOARTHROPATHY ON (B)(6) 2019. THE SURGEON USED THE REAMER (212861001) FOR SCRAPING THE SCAPULA. IT TOOK TIME FOR THE SCRAPING BECAUSE THE REAMER WAS NOT SHARP ENOUGH. THE PROCEDURE WAS DELAYED LESS THAN 30 MINUTES. THERE WAS NO HARM TO THE PATIENT. THE DEVICE WAS THE FIRST USE WHEN THE ISSUE OCCURRED.

    Patient problems: Not Applicable

    MAUDE report 9156522 ↗

Other REAMER devices

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Sources and updates

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