GLOBAL ADVANTAGE 1128-52-110Recalls & reported problems

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 10603295005223), received between Dec 19, 2017 and Jan 29, 2026 — classified as 14 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (3 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 18, 2026.

Most reported problems

Recent adverse event reports

The 14 most recent of 14 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 24210839 ↗
• InjuryJan 13, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO PAIN. SURGEON CONVERTED SHOULDER FROM HEMI TO TOTAL SHOULDER ARTHROPLASTY. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Pain

  MAUDE report 21142690 ↗
• InjuryAug 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO RULE OUT INFECTION. DOI: (B)(6) 2018, DOR: (B)(6) 2024 , AFFECTED SIDE : LEFT SHOULDER.

  Patient problems: Unspecified Infection

  MAUDE report 20086034 ↗
• InjuryApr 15, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION GLOBAL ADVANTAGE HEMI ARTHROPLASTY. PATIENT PRESENTED TO SURGEON WITH PAIN. GLOBAL ADVANTAGE STEM AND HEAD REMOVED AND REVISION TO DJO REVERSE TOTAL SHOULDER ARTHROPLASTY PERFORMED. DOI: (B)(6) 2004; DOE: (B)(6) 2024.

  Patient problems: Pain; Unspecified Tissue Injury

  MAUDE report 19106289 ↗
• InjuryJan 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAS A ROTATOR CUFF TEAR. DOI: (B)(6) 2016. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 18448397 ↗
• InjuryAug 1, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO HEMI SHOULDER ARTHROPLASTY PAIN. IT WAS REVISED TO A TOTAL REVERSE ARTHROPLASTY AND THERE WERE NO SIGNS OF INFECTION. IT WAS UNKNOWN IF THERE WAS ANY SURGICAL DELAY. DOI: (B)(6) 2020. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Pain

  MAUDE report 17434290 ↗
• InjuryJul 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ORIGINAL SURGERY RIGHT HEMI ARTHROPLASTY USING GLOBAL ADVANTAGE STEM AND HEAD. REVISION SURGERY (B)(6) 2021. (B)(6). REASON FOR REVISION -GLENOID EROSION.

  Patient problems: Pocket Erosion

  MAUDE report 12161124 ↗
• InjuryFeb 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS PAIN, INSTABILITY AND LOOSENING OF THE GLENOID COMPONENT AT THE CEMENT TO IMPLANT INTERFACE. COMPETITOR CEMENT WAS USED. DOI: (B)(6) 2018, DOR: (B)(6) 2021, LEFT SHOULDER.

  Patient problems: Joint Laxity; Pain

  MAUDE report 11321986 ↗
• InjuryJul 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT STATED THAT A YEAR AFTER HIS SURGERY, HE FELL. A TORN SUBSCAP WAS DISCOVERED AS THE REASON FOR A LOOSE COMPONENT. GLENOID WAS WORN DUE TO THIS SOFT TISSUE LAX AND WAS REMOVED. HEAD WAS ALSO REPLACED WITH A LARGER HEAD TO HELP TIGHTEN THE SPACE. DOI: (B)(6) 2016, DOR: (B)(6) 2020, RIGHT SHOULDER.

  Patient problems: Fall; No Code Available

  MAUDE report 10320088 ↗
• InjuryAug 27, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE AFFECTED SIDE IS THE RIGHT SHOULDER.

  Patient problems: Joint Disorder; No Code Available; Pain

  MAUDE report 8934951 ↗
• InjuryJul 10, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS PAIN AND LIMITED RANGE OF MOTION. DOI: (B)(6) 2016. DOR: (B)(6) 2018. LEFT SHOULDER.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 7673223 ↗
• InjuryFeb 28, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE PATIENT WAS REVISED TO ADDRESS PAIN AND INSTABILITY. SURGEON REMOVED ANTERIOR OSTEOPHYTES. DOI: UNKNOWN; DOR: (B)(6) 2018; LEFT SHOULDER.

  Patient problems: Pain

  MAUDE report 7302691 ↗
• 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 7205105 ↗
• InjuryDec 19, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  IMPLANT REMOVED DUE TO INFECTION. PATIENT CONSEQUENCE?: UNKNOWN. IS THE INFORMATION BEING SUBMITTED FOR THIS COMPLAINT ALL THE DETAILS THAT ARE KNOWN/AVAILABLE REGARDING THIS EVENT?: YES.

  Patient problems: Unspecified Infection

  MAUDE report 7128351 ↗