GLOBAL ADVANTAGE 2128-61-017Recalls & reported problems
Depuy (Ireland) · GLOBAL ADVANTAGE GLENOID GRASPER · Class 1
All models of GLOBAL ADVANTAGE (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295089391), received between Oct 19, 2021 and Dec 15, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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
- Device-Device Incompatibility2
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 15, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE GRASPER WILL NOT HOLD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15986933 ↗MalfunctionNov 30, 2022Material Deformation; Material Deformation
IT WAS REPORTED THAT THE STEM TRIAL HAD THE LITTLE PIECE FROM THE STEM WRENCH BREAK OFF INTO THE BOTTOM THE STEM TRIAL SO BOTH THE STEM TRIAL AND WRENCH ARE BROKEN. THE GLENOID SIZER HAD A SLIGHT CRACK THAT THE SURGEON NOTICED AND THE GLENOID INSERTER GOT BENT AS THE SURGEON WAS IMPLANTING THE GLENOID. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15887731 ↗MalfunctionOct 19, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE GLENOID GRASPER WOULD NOT LATCH ONTO THE IMPLANT ANYMORE. THE SURGEON USED IT TO TAKE OUT THE GLENOID IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12656253 ↗
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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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