GLOBAL 1137-86-025Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ENDURON PE SHOULDER - GLENOID PEG SIZE 48 · Class 2 · Implant
All models of GLOBAL (20)
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 10603295007265), received between May 15, 2018 and Nov 14, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Failure To Adhere Or Bond” (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
- Failure To Adhere Or Bond1
- Loss of or Failure to Bond1
- Naturally Worn1
Patient problems
- No Code Available2
- Not Applicable1
- Pain1
- Unspecified Infection1
- 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 14, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
LEFT SHOULDER REVISION - ANATOMIC SHOULDER REPLACEMENT COMPLETED 2010 ON THE SUNSHINE COAST (EXACT DATE AND SURGEON UNKNOWN). DISEASE PROGRESSION HAS LEAD TO ROTATOR CUFF FAILURE, SUSPECTED LOOSENING OF GLENOID COMPONENT - SURGEON PLANNED TO REMOVE ANATOMIC PROSTHESIS AND IMPLANT REVERSE PROSTHESIS. GLENOID AND HUMERAL HEAD COMPONENTS WERE ABLE REMOVED BUT THE HUMERAL STEM WAS TOO WELL FIXED TO EXPLANT. SURGEON OPTED TO PUT ON A CTA HEAD INSTEAD AS THE MOST SUITABLE OPTION FOR THE PATIENT.
Patient problems: Unspecified Tissue Injury
MAUDE report 15788021 ↗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 10985121 ↗InjuryApr 26, 2019Naturally Worn; Naturally Worn
REASON FOR REVISION: CUFF FAILURE RENDERING TOTAL ANATOMICAL REPLACEMENT INAPPROPRIATE FOR PATIENT NEEDS. 9 MONTHS POST IMPLANTATION CUFF FAILURE RESULTED IN TOTAL ANATOMIC SHOULDER CONVERSION TO REVERSE SHOULDER PROSTHESIS. BASED ON ANATOMIC CHANGES AND NOT ON FAILURE OF IMPLANTED PROSTHESIS TO FUNCTION AS INTENDED. GLENOID PEG SHOWS SIGNS OF SUPERIOR WEAR. ALL PROSTHESIS SUCCESSFULLY REMOVED WITHOUT COMPLICATION.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 8554816 ↗InjuryMay 15, 2018Failure To Adhere Or Bond; Failure To Adhere Or Bond
DER STATES THAT THE PATIENT'S ROTATOR CUFF FAILED SO THE SURGEON PULLED EVERYTHING OUT AND CONVERTED TO A DJO REVERSE. THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE GLENOID COMPONENT AT THE BONE TO CEMENT AND CEMENT TO IMPLANT INTERFACE. DEPUY CEMENT WAS USED. DOI: UNKNOWN. DOR: (B)(6) 2018. LEFT SHOULDER.
Patient problems: No Code Available; Not Applicable
MAUDE report 7513793 ↗
Other PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED devices
- Equinoxe 320-42-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-38-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-42-03Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls87 reports
- Equinoxe 320-38-03Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls43 reports
- Equinoxe 320-42-13Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls41 reports
- Equinoxe 320-10-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented132 reports
- Equinoxe 320-36-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls27 reports
- Equinoxe 320-42-10Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls14 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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