GLOBAL AP 1130-48-600Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP HUMERAL HEAD ECCENTRIC SIZE 48 x 15 · Class 2 · Implant
All models of GLOBAL AP (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295006077), received between Sep 14, 2020 and Sep 14, 2021 — 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
Device problems
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Pain2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Discomfort1
- Limited Mobility Of The Implanted Joint1
- Muscular Rigidity1
- No Code Available1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 14, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
RIGHT TOTAL SHOULDER REMOVED FOR PROSTALAC SPACER BECAUSE OF INFECTION. IMPLANTED APPROXIMATELY 10 YEARS AGO. NO OTHER INFORMATION AVAILABLE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 12468706 ↗InjuryDec 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT UNDERWENT A PARTIAL REVISION RIGHT SHOULDER REPLACEMENT. THE GLENOID COMPONENT WAS REMOVED AND THE NECK TAPER AND HEAD WAS CHANGED.
Patient problems: Pain
MAUDE report 10985110 ↗InjurySep 14, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PRIMARY ANATOMIC SHOULDER REPLACEMENT ON (B)(6) 2014. LAST 2 YEARS, INCREASING STIFFNESS IN SHOULDER JOINT, WITH MODERATE DEGREE OF DISCOMFORT. CURRENTLY UNABLE TO ABDUCT ARM PAST LEVEL OF SHOULDER. SURGEON STATED GLENOID WAS A B2 GLENOID AT THIS SURGERY. ALL COMPONENTS WELL FIXED, NO EVIDENCE OF INFECTION AND WITH CONCENTRIC WEAR ON GLENOID POLY COMPONENT. ALL COMPONENTS REMOVED (HUMERAL EPISIOTOMY REQUIRED); AND A COMPETITOR RSA PROSTHESIS (ZIMMER COMPREHENSIVE) IMPLANTED, USING AUGMENTED GLENOID COMPONENT.
Patient problems: Discomfort; Limited Mobility Of The Implanted Joint; Muscular Rigidity; No Code Available; Pain
MAUDE report 10528774 ↗
Other PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED devices
- DJO SURGICAL 509-02-032Encore Medical, L.P. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED364 reports
- DELTA XTEND 130790036Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED171 reports
- DELTA XTEND 130770018Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED159 reports
- TRIGEN 71118200Smith & Nephew, Inc. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED123 reports
- DJO SURGICAL 509-02-432Encore Medical, L.P. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED119 reports
- DELTA XTEND 130738206Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED116 reports
- COMPREHENSIVE SHOULDER SYSTEM 113633Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED2 recalls4 reports
- DELTA XTEND 130742206Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED99 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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