GLOBAL ADVANTAGE 2128-62-120Recalls & reported problems
Depuy (Ireland) · GLOBAL ADVANTAGE + CUFF GUIDE LEFT · 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 10603295089827), received between Jun 15, 2021 and Aug 7, 2024 — classified as 2 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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 7, 2024Device-Device Incompatibility; Device-Device Incompatibility
WHEN ATTEMPTING TO PIN THE ANATOMIC RESECTION GUIDE, THE LEGEND II FIXATION PIN BECAME STUCK IN THE PIN HOLE AND WAS UNABLE TO BE REMOVED. THE SURGEON PINNED THE CUTTING GUIDE USING THE REMAINING PINHOLE. THERE WAS NO IMPACT TO THE PATIENT, AND NO DELAY TO SURGERY. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19929224 ↗MalfunctionJun 15, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE GLOBAL UNITE ANATOMIC CUTTING GUIDE WAS FOUND TO HAVE A FIXATION PIN STUCK IN THE GUIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11999826 ↗
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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