GLOBAL ADVANTAGE 1137-14-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295007173), received between Sep 8, 2017 and Jan 29, 2026 — classified as 6 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryJan 29, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO FAILED ROTATOR CUFF, RESULTING IN THE IMPLANTATION OF A REVERSE SHOULDER SYSTEM. DOI: (B)(6) 2015. DOR: (B)(6) 2026. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 24210838 ↗
• InjuryJan 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD AN ANATOMIC IN AND WAS REVISED TO A REVERSE. ANATOMIC IMPLANTS WERE EXPLANTED. NO SURGICAL DELAY. NO PATIENT CONSEQUENCE. DOI: (B)(6) 2020 DOR: (B)(6) 2024 AFFECTED SIDE: UNKNOWN SHOULDER SIDE.

  Patient problems: Joint Laxity

  MAUDE report 21243370 ↗
• InjuryJul 25, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS REASON FOR REVISION: REVISION DUE TO PAIN.

  Patient problems: Pain

  MAUDE report 19833748 ↗
• InjuryAug 6, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS PAINFUL SHOULDER. LACK OF FUNCTION, CONVERTING TO REVERSE. DOI: 2008. DOR: UNKNOWN, RIGHT SHOULDER.

  Patient problems: No Code Available; Pain

  MAUDE report 8865809 ↗
• InjuryJan 19, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE PATIENT WAS REVISED TO ADDRESS JOINT PAIN AND EROSION OF ROTATOR CUFF. THE SURGEON REMOVED STEM AND HEAD, REPLACED WITH ZIMMER REVERSE SHOULDER. DOI: UNKNOWN; DOR: (B)(6) 2017; RIGHT SHOULDER.

  Patient problems: Pain

  MAUDE report 7205107 ↗
• InjurySep 8, 2017Loss of Osseointegration; Loss of Osseointegration

  DER STATES THAT PATIENT HAD PAINFUL SHOULDER, WITH RADIOGRAPHIC EVIDENCE OF HUMERAL STEM LOOSENING AT THE BONE TO IMPLANT INTERFACE. IT WAS ALSO REPORTED THAT THE ALLOGRAFT BONE WAS USED IN HUMERAL CANAL TO ENHANCE ROTATIONAL STABILITY.

  Patient problems: No Information

  MAUDE report 6851957 ↗