GLOBAL ADVANTAGE 1137-10-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295007128), received between Jan 5, 2018 and Jan 10, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

Recent adverse event reports

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

• InjuryJan 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS LOST FUNCTION OF SUBSCAP AND WAS CONVERTED TO A REVERSE SHOULDER FROM ANOTHER COMPANY. COULD NOT GET A COMPLETE SET OF RECORDS. PATIENT HAD TOTAL SHOULDER DONE IN 2010. DOI: (B)(6) 2010; DOR: (B)(6) 2019 RIGHT SHOULDER.

  Patient problems: No Code Available

  MAUDE report 9577415 ↗
• InjuryJan 5, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS INFECTION. DOI- UNKNOWN. DOR: (B)(6) 2017. AFFECTED SIDE: LEFT SHOULDER.

  Patient problems: Unspecified Infection

  MAUDE report 7169418 ↗