GLOBAL AP 1130-52-510Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP HUMERAL HEAD SIZE 52 x 18 · Class 2 · Implant
All models of GLOBAL AP (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295006237), received between Jul 7, 2020 and Feb 3, 2025 — classified as 2 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Limited Mobility Of The Implanted Joint1
- No Code Available1
- Pain1
- Unspecified Tissue Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION WAS RECEIVED AND STATES THAT: 1. CAN YOU PLEASE ADVISE ON THE SURGEON¿S OPINION FOR THE REASON OF THE REVISION SURGERY? FAILED ROTATOR CUFF. 2. WAS IT RELATED TO PATIENT FACTORS OR DEVICE RELATED? PATIENT. 4. PLEASE CONFIRM IF ALL BELOW COMPONENTS WERE EXPLANTED? AND DISCARDED? EXPLANTED AND LEFT AT HOSPITAL. 5. WAS THERE ANY ALLEGATION AGAINST THE METAGLENE GUIDE PIN DIA 2.5MM? N/A.
Patient problems: Unspecified Tissue Injury
MAUDE report 21291999 ↗InjuryJul 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT PRESENT IN THE DOCTOR'S OFFICE WITH A PAINFUL LEFT SHOULDER AND A DECREASE IN RANGE OF MOTION. SURGEON ORDERED A SERIES OF STUDIES AND FORMED THE OPINION THAT THE INDEX GLENOID COMPONENT WAS LOOSE. THE SURGEON REVISED THE SHOULDER. UPON EXPOSURE TO THE JOINT SPACE, DR. REMOVED THE 52X18 STANDARD HUMERAL HEAD FOR THE AP SHOULD SYSTEM, AND THE 135 TAPERED SPACER WITH THE STANDARD HEAD REMOVAL FORK IN THE GLOBAL AP TRAYS. THE SIZE 10 GLOBAL AP STANDARD STEM WAS KEPT IMPLANTED. SURGEON THEN EASILY REMOVED THE 52 ANCHOR PEG GLENOID WITH A PAIR OF KOCHERS. DUE TO BONE LOSS, SURGEON THEN IMPLANTED A COMPETITIVE GLENOID. NO INSTRUMENTATION BROKE DURING SURGERY AND THERE WERE NO DELAYS.
Patient problems: Limited Mobility Of The Implanted Joint; No Code Available; Pain
MAUDE report 10240917 ↗
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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