GLOBAL 1137-87-025Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ENDURON PE SHOULDER - GLENOID PEG SIZE 52 · Class 2 · Implant
All models of GLOBAL (20)
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 10603295007289), received between Mar 3, 2021 and Aug 10, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 reports).
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
- Loss of or Failure to Bond2
- Naturally Worn2
Patient problems
- Insufficient Information3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryAug 10, 2022Loss of or Failure to Bond; Naturally Worn; Loss of or Failure to Bond; Naturally Worn
REVISION OF ANATOMIC TO REVERSE SHOULDER. GLENOID LOOSE /WORN. ORIGINAL SURGERY 2004. DOI: 2004; DOR: (B)(6) 2022; UNKNOWN SIDE.
Patient problems: Insufficient Information
MAUDE report 15197684 ↗InjuryMay 5, 2021Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED TO ADDRESS ECCENTRIC POLY WEAR. DOI: UNKNOWN DOR: (B)(6) 2021 LEFT KNEE.
Patient problems: Insufficient Information
MAUDE report 11778433 ↗InjuryMar 3, 2021Loss of or Failure to Bond; Loss of or Failure to Bond
ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE AFFECTED SIDE WAS THE RIGHT SHOULDER.
Patient problems: Insufficient Information
MAUDE report 11405242 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page