GLOBAL 1136-41-025Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL ANCHOR PEG GLENOID SIZE 44mm CEMENTED · 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 10603295006961), received between Mar 1, 2018 and Oct 2, 2019 — classified as 4 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
- Loose or Intermittent Connection1
- Loosening of Implant Not Related to Bone-Ingrowth1
- Naturally Worn1
Patient problems
- No Code Available2
- Not Applicable1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryOct 2, 2019Loss of or Failure to Bond; Loosening of Implant Not Related to Bone-Ingrowth; Loss of or Failure to Bond; Loosening of Implant Not Related to Bone-Ingrowth
THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE GLENOID COMPONENT AT THE UNKNOWN INTERFACE. UNKNOWN CEMENT WAS USED. IT WAS ALSO REPORTED THE ANCHOR PEG GLENOID WAS REMOVED. DOI: (B)(6) 2007. DOR: (B)(6) 2019, RIGHT SHOULDER.
Patient problems: No Code Available
MAUDE report 9144708 ↗InjuryJan 2, 2019Naturally Worn; Naturally Worn
PATIENT REVISED DUE TO DISASSOCIATION OF IMPLANTS.
Patient problems: No Code Available
MAUDE report 8208837 ↗InjuryAug 30, 2018Loss of or Failure to Bond; Loss of or Failure to Bond
REVISION GLOBAL ADVANTAGE, THE SURGEON; (B)(6). PRIMARY IMPLANT DATE 2008. GLOBAL ADVANTAGE IN SITU, GLENOID COMPONENT LOOSE - AS PER SURGEON. STEM WELL FIXED - AS PER SURGEON. LOOSE DUE TO LENGTH OF TIME IN SITU - AS PER SURGEON. PATIENT HAD A PREVIOUS SHOULDER INJURY IN 1993. GLENOID REMOVED IN ONE PIECE. MULTIPLE SPECIMENS TAKEN, IMAGES UPLOADED TO UNITY. PATIENT (B)(6).
Patient problems: Not Applicable
MAUDE report 7832810 ↗InjuryMar 1, 2018Loose or Intermittent Connection; Loose or Intermittent Connection
PRIMARY SURGERY DATE (B)(6) 2007. REVISION FOR: PAIN AND INSTABILITY DUE TO A LOSE GLENOID COMPONENT. THE SURGEON STATED THAT THE GLENOID COMPONENT WAS LOSE AND HAD TO BE REMOVED. THE PATIENTS ROTATOR CUFF TENDON HAD TO BE REPAIRED DURING THE REVISION SURGERY. THE SURGEON REPLACED THE EXPLANTED WITH THE SAME SIZE NEW IMPLANTS. DOI: (B)(6) 2007 DOR: (B)(6) 2018 UNKNOWN SHOULDER.
Patient problems: Pain
MAUDE report 7305855 ↗
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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