GLOBAL ADVANTAGE 2128-44-221Recalls & reported problems
Depuy (Ireland) · GLOBAL ADVANTAGE + ECCENTRIC HUMERAL HEAD TRIAL 44 x 21 · Class 1
All models of GLOBAL ADVANTAGE (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295088783), received between Nov 20, 2017 and Nov 20, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Component Missing” (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
- Component Missing2
Patient problems
- No Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 20, 2017Component Missing; Component Missing
IT WAS REPORTED THAT WHILE INSPECTING THE TRIALS, HE FOUND THAT THE SCREW THAT IS IN EACH ONE OF THE TRIALS IS MISSING. IT WAS NOTICED IN THE DISTRIBUTION CENTER.
Patient problems: No Information
MAUDE report 7046346 ↗MalfunctionNov 20, 2017Component Missing; Component Missing
IT WAS REPORTED THAT WHILE INSPECTING THE TRIALS, HE FOUND THAT THE SCREW THAT IS IN EACH ONE OF THE TRIALS IS MISSING. IT WAS NOTICED IN THE DISTRIBUTION CENTER.
Patient problems: No Information
MAUDE report 7046333 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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