GLOBAL APG+ 2230-10-031Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ LOW PROFILE CENTRAL REAMER SIZE 48/52/56 RU · Class 1
All models of GLOBAL APG+ (34)
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 10603295104766), received between Mar 5, 2020 and Dec 9, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (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
- Material Deformation2
- Naturally Worn2
- Dull, Blunt1
- Failure to Cut1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 9, 2022Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
MINIMAL DELAY IN THE PROCEDURE (TIME TAKEN TO OPEN A DIFFERENT TRAY). NO ADVERSE OUTCOME FOR THE PATIENT AS SPARE INSTRUMENT TRAY AVAILABLE AT THE HOSPITAL. PROCEDURE ¿ TOTAL RIGHT ANATOMIC SHOULDER REPLACEMENT USING GLOBAL ADVANTAGE AND GLOBAL ANCHOR PEG GLENOID +.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15951166 ↗MalfunctionDec 9, 2022Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
MINIMAL DELAY IN THE PROCEDURE (TIME TAKEN TO OPEN A DIFFERENT TRAY). NO ADVERSE OUTCOME FOR THE PATIENT AS SPARE INSTRUMENT TRAY AVAILABLE AT THE HOSPITAL. PROCEDURE ¿ TOTAL RIGHT ANATOMIC SHOULDER REPLACEMENT USING GLOBAL ADVANTAGE AND GLOBAL ANCHOR PEG GLENOID +.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15950939 ↗MalfunctionMar 5, 2020Dull, Blunt; Failure to Cut; Material Twisted/Bent; Dull, Blunt; Failure to Cut; Material Twisted/Bent
SURGEON ADVISED THAT THE LARGE LOW PROFILE CENTRAL REAMER: 48/52/56 IS COMPLETELY BLUNT. THERE WAS NO IMPACT ON THE PATIENT. THE SURGEON JUST REPORTED THAT THE REAMER WAS BLUNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9795137 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 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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