GLOBAL 1136-44-025Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ANCHOR PEG GLENOID SIZE 56mm CEMENTED · Class 2 · Implant
All models of GLOBAL (20)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295007029), received between Oct 2, 2019 and Oct 2, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- No Code Available1
- Osteolysis1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 2, 2019Adverse Event Without Identified Device or Use Problem; Loosening of Implant Not Related to Bone-Ingrowth; Adverse Event Without Identified Device or Use Problem; Loosening of Implant Not Related to Bone-Ingrowth
PRIMARY SURGERY: (B)(6) 2006. REVISION SURGERY WAS CARRIED OUT DUE TO GLENOID COMPONENT LOOSENING AND PAIN. THE SURGEON REMOVED THE HUMERAL HEAD AND THE LOOSE GLENOID COMPONENT AND REPLACED WITH NEW IMPLANTS. OSTEOLYSIS MEDIAL TO THE GLENOID COMPONENT WAS NOTED, SPECIMENS HARVESTED FOR CULTURE. THE SURGEON DID INDICATE THAT THE PATIENT IS CURRENTLY BEING TREATED FOR CANCER AND THAT THE OSTEOLYTIC REACTION MEDIAL TO THE GLENOID COMPONENT MAY BE AS A RESULT OF THIS TREATMENT OR THE DISEASE. NO AE REPORTED, NO DELAY IN THE SURGERY. RELEVANT PATIENT PRE-EXISTING CONDITIONS: TREATED FOR LUNG CANCER.
Patient problems: No Code Available; Osteolysis; Pain
MAUDE report 9146964 ↗
Other PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED devices
- Equinoxe 320-38-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-42-00Exactech, 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 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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