GLOBAL ADVANTAGE 2128-01-014Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295088004), received between Mar 15, 2021 and Nov 28, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 28, 2022Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMER WAS DULL. NO SURGICAL DELAY WAS THERE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15873096 ↗
• MalfunctionMar 15, 2021Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE SHOULDER REAMERS ARE DULL AND NEED TO BE REPLACED. DID NOT MAKE CASE GO LONGER. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11489645 ↗