GLOBAL AP 1130-14-000Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP STANDARD STEM SIZE 14 147mm · Class 2 · Implant
All models of GLOBAL AP (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295005551), received between Nov 8, 2017 and Mar 31, 2026 — classified as 3 injuries, 1 malfunction.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Insufficient Device Problem Information1
- Packaging Problem1
Patient problems
- Pain2
- Loss of Range of Motion1
- Muscular Rigidity1
- No Known Impact Or Consequence To Patient1
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2026Adverse Event Without Identified Device or Use Problem
SUBJECT ID: (B)(6), STUDY NO: (B)(4). CLINICAL ADVERSE EVENT RECEIVED FOR CONCERN FOR GLENOID COMPONENT LOOSENING/POLY WEAR RESULTING IN PAIN AND DYSFUNCTION IN RIGHT SHOULDER DEVICE AND PROCEDURE (RELATEDNESS): DEVICE RELATED: PROBABLE, PROCEDURE RELATED: PROBABLE, DATE OF EVENT: 1 JAN 2026, DATE OF IMPLANT: (B)(6) 2013, DATE OF REVISION: NO INFORMATION PROVIDED, DEVICE LOCATION: RIGHT SHOULDER. TREATMENT/IMPACT: ASPIRATION: YES DEPUY SYNTHES PRODUCTS USED: CATALOG NUMBER: 113643026 LOT NUMBER: 348444 COMPONENT TYPE: ANCHOR DESCRIPTION: PREMIERON XLINKED GLENOID ANCHOR PEG 52MM. CATALOG NUMBER: 113014000 LOT NUMBER: 351106 COMPONENT TYPE: STEM DESCRIPTION: GLOBAL HUMERAL STEM SZ 14. CATALOG NUMBER: 110052520 LOT NUMBER: FK1JD1 COMPONENT TYPE: HEAD DESCRIPTION: GLOBAL UNITE HEAD 52X21 STD. CATALOG NUMBER: 113002000 LOT NUMBER: 371961 COMPONENT TYPE: TAPER ASSEMBLY DESCRIPTION: GLOBAL AP TAPER ASSEMBLY 135 DEGREE.
Patient problems: Loss of Range of Motion; Pain
MAUDE report 24743529 ↗InjuryJan 28, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PT IS BEING REVISED FOR CHRONIC PAIN AND STIFFNESS.
Patient problems: Muscular Rigidity; Pain
MAUDE report 11247535 ↗MalfunctionSep 25, 2018Packaging Problem; Packaging Problem
NO SECONDARY SEAL AROUND IMPLANT AND IMPLANT STICKERS LOOSE IN THE BOX. NO STERILIZATION EVIDENCE ATTACHED TO INNER IMPLANT PACKAGING.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7905506 ↗InjuryNov 8, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
THE PATIENT WAS REVISED TO ADDRESS INFECTION OF THE GLOBAL AP IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 7009004 ↗
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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