GLOBAL AP 1130-08-200Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP POROCOAT STANDARD STEM SIZE 8 126mm · 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
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295005483), received between Jan 15, 2020 and Nov 10, 2025 — classified as 4 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Device Dislodged or Dislocated1
- Loss of Osseointegration1
- Use of Device Problem1
Patient problems
- Pain2
- Inadequate Osseointegration1
- No Code Available1
- Unspecified Tissue Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryNov 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT UNDERWENT REVISION FROM A GLOBAL AP TO A DELTA EXTEND DUE TO CUFF TEAR AND SUPERIOR MIGRATION OF THE HUMERUS.
Patient problems: Unspecified Tissue Injury
MAUDE report 23512096 ↗InjuryJun 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT BEGAN EXPERIENCING PAIN. IMPLANTS WERE IN GOOD CONDITION. THE CEMENT MANUFACTURER WAS MARKED AS DEPUY. AFFECTED SIDE: UNKNOWN SHOULDER SIDE.
Patient problems: Pain
MAUDE report 22140881 ↗InjuryMar 5, 2024Use of Device Problem; Use of Device Problem
ADDITIONAL INFORMATION WAS RECEIVED: A. WAS THERE ANY PATIENT CONSEQUENCE RELATED TO THE EVENT. - WE REVISED THE SHOULDER AS DESCRIBED IN THE PC. B. WAS THERE ANY SURGICAL DELAY RELATED TO THE EVENT? - SURGICAL DELAY QUESTION IS NOT REALLY APPLICABLE AS THE ENTIRE SURGERY WAS A REVISION.
Patient problems: Pain
MAUDE report 18836369 ↗InjuryJan 15, 2020Loss of Osseointegration; Device Dislodged or Dislocated; Loss of Osseointegration; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF NON-CEMENTED STEM. THE TAPER DID NOT ENGAGE BETWEEN THE HEAD AND THE STEM. DOI: UNKNOWN. DOR: (B)(6) 2020; UNKNOWN SIDE.
Patient problems: Inadequate Osseointegration; No Code Available
MAUDE report 9592676 ↗
Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED devices
- COMPREHENSIVE SHOULDER SYSTEM 113629Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall2 reports
- COMPREHENSIVE SHOULDER SYSTEM 113617Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall1 report
- Comprehensive® Shoulder System 113607Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall1 report
- BIO-MODULAR SHOULDER SYSTEM 113865Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 reports
- COPELAND SHOULDER SYSTEM 11-114648Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 reports
- COMPRESS DEVICE 178787Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 reports
- BIO-MODULAR SHOULDER SYSTEM 113863Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 reports
- BIO-MODULAR SHOULDER SYSTEM 113867Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 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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