GLOBAL APG+ 2230-00-031Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ LOW PROFILE CENTRAL REAMER SIZE 48/52/56 · Class 1
All models of GLOBAL APG+ (34)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295103042), received between Apr 2, 2019 and Oct 11, 2023 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (5 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
- Failure to Cut5
- Dull, Blunt2
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Consequences Or Impact To Patient2
- Insufficient Information1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 11, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GLENOID REAMER IS DULL.
Patient problems: Insufficient Information
MAUDE report 17913732 ↗MalfunctionNov 30, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE 52 +0 PEG WORN DOWN. DOES NOT ATTACHED TO HANDLE PROPERLY, NO PIECES. 48/52/56 REAMERS WAS DULL. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15888400 ↗MalfunctionNov 30, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE 52 +0 PEG WORN DOWN. DOES NOT ATTACHED TO HANDLE PROPERLY, NO PIECES. 48/52/56 REAMERS WAS DULL. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15888391 ↗MalfunctionNov 30, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE 52 +0 PEG WORN DOWN. DOES NOT ATTACHED TO HANDLE PROPERLY, NO PIECES. 48/52/56 REAMERS WAS DULL. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15888345 ↗MalfunctionNov 30, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE 52 +0 PEG WORN DOWN. DOES NOT ATTACHED TO HANDLE PROPERLY, NO PIECES. 48/52/56 REAMERS WAS DULL. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15888225 ↗MalfunctionApr 2, 2019Dull, Blunt; Dull, Blunt
THE REAMER BLADES ARE DULL. NO SURGICAL DELAY HAPPEN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8473357 ↗MalfunctionApr 2, 2019Dull, Blunt; Dull, Blunt
THE REAMER BLADES ARE DULL. NO SURGICAL DELAY HAPPEN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8473343 ↗
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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