GLOBAL 1136-44-026Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ANCHOR PEG GLENOID PREMIERON X-LINKED PE SIZE 56mm · Class 2 · Implant
All models of GLOBAL (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295007036), received between Aug 7, 2018 and Sep 30, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Naturally Worn” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
- Naturally Worn1
Patient problems
- Unspecified Tissue Injury2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Not Applicable1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem
It was reported that patient had left anatomic total shoulder approximately 10 years ago. Original date of surgery and hospital are unknown. Patient developed rotator cuff arthropathy and was revised to a reverse total shoulder.DOI: Unknown.DOR: (b)(6) 2026.Affected side: Left shoulder.
Patient problems: Unspecified Tissue Injury
MAUDE report 50945102 ↗InjuryJul 29, 2026Adverse Event Without Identified Device or Use Problem
Patient was revised due to failed rotator cuff, conversion to Delta Xtend. DOI: (b)(6)2018.DOR: (b)(6)2026.Affected side: Right shoulder.
Patient problems: Unspecified Tissue Injury
MAUDE report 50072417 ↗InjuryJun 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SINGLE STAGE REVISION OF GLOBAL UNITE ANATOMIC SHOULDER REPLACEMENT DUE TO CONFIRMED INFECTION. HUMERAL HEAD, PROXIMAL BODY AND GLENOID COMPONENT REMOVED, AREA FLUSHED, NEW IMPLANTS PUT IN. DOI: (B)(6) 2020, DOR: (B)(6) 2021, RIGHT SHOULDER.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11945818 ↗InjuryAug 7, 2018Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SURGEON REMOVED GLOBAL UNITE IMPLANTS DUE TO MALPOSITIONED COMPONENTS AND WORN GLENOID. SURGEON CHOOSE TO IMPLANT A REVERSE SHOULDER CONSTRUCT. DOI: UNKNOWN; DOR: (B)(6) 2018; RIGHT SHOULDER.
Patient problems: Not Applicable
MAUDE report 7756652 ↗
Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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