GLOBAL ADVANTAGE 1128-65-060Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ADVANTAGE CTA HEAD SIZE 52mm x 23mm · Class 2 · Implant
All models of GLOBAL ADVANTAGE (47)
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 10603295005346), received between Mar 23, 2018 and Feb 5, 2021 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
- Malposition of Device1
Patient problems
- Pain2
- Loss of Range of Motion1
- No Code Available1
- Not Applicable1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 5, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED TO ADDRESS LACK OF FUNCTION AND PAIN. NO SURGICAL DELAY. THE PATIENT HAD NO UPWARD MOBILITY WITH THEIR ARM. DOI: 10-11 YEARS AGO, DOR: (B)(6) 2021, LEFT SHOULDER.
Patient problems: Loss of Range of Motion; Pain
MAUDE report 11286207 ↗InjuryMar 10, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS INFECTION AND LOOSENING OF THE HUMERAL HEAD . HE WAS TAKEN TO THE OR TODAY FOR REMOVAL OF IMPLANTS, I&D, AND PLACEMENT OF ANTIBIOTIC SPACER. NO OTHER INFORMATION. DOI: UNKNOWN; DOR: (B)(6) 2020; RIGHT SHOULDER.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 9815012 ↗InjuryMar 23, 2018Malposition of Device; Malposition of Device
DER STATES PATIENT PRESENTED WITH A PAINFUL AND UNSTABLE SHOULDER. ACCORDING TO THE PATIENT THIS INSTABILITY HAS OCCURRED SINCE ORIGINAL SURGERY. IN THE OR THE DOCTOR NOTICED THE IMPLANTS WERE NOT AT A TRADITIONAL 30 DEGREES OF RETROVERSION, BUT SLIGHTLY ANTEVERTED. DOI: (B)(6) 2010; DOR: (B)(6) 2018; RIGHT SHOULDER.
Patient problems: Not Applicable; Pain
MAUDE report 7365713 ↗
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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