GLOBAL ADVANTAGE 1128-56-110Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295005278), received between Aug 13, 2019 and May 22, 2023 — classified as 3 injuries.

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMay 22, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED FOR CONVERSION FROM HEMI TO TOTAL DUE TO GLENOID CYST. DOI: UNKNOWN; DOR: (B)(6) 2023; AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Cyst(s)

  MAUDE report 16973455 ↗
• InjuryMar 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAIN AND INSTABILITY. IT IS UNKNOWN WHERE OR WHEN THE ORIGINAL SURGERY WAS DONE. THE SURGEON WENT IN AND PERFORMED A GLENOID REPLACEMENT ON A NATIVE GLENOID. THEN HE LOOKED AT THE PLACEMENT AND STABILITY OF THE HUMERAL COMPONENT. THE SURGEON ONLY NEEDED TO CHANGE THE HUMERAL HEAD AS THE STEM WAS SOLID. DOI: UNKNOWN; DOR: (B)(6) 2022; AFFECTED SIDE: LEFT SHOULDER.

  Patient problems: Joint Laxity; Pain

  MAUDE report 13950071 ↗
• InjuryAug 13, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS PAIN. DOI: UNKNOWN. DOR: (B)(6) 2019, RIGHT SHOULDER.

  Patient problems: No Code Available; Pain

  MAUDE report 8888908 ↗