GLOBAL APG+ 2236-00-008Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ ACCESS REAMER SIZE 40 · 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 10603295105756), received between Jul 10, 2019 and Jul 24, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (3 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
- Dull, Blunt3
- Failure to Cut2
- Material Deformation2
- Material Twisted/Bent1
Patient problems
- No Consequences Or Impact To Patient3
- No Code Available2
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 24, 2020Dull, Blunt; Failure to Cut; Material Deformation; Dull, Blunt; Failure to Cut; Material Deformation
IT WAS REPORTED THAT THE 38 POLY TRIALS ARE DAMAGED WITH SCARS AND MISSING PLASTIC IN AREAS SURGEON AND SPD WANTED THEM REPLACED. PROTECTIVE PLATE IS BENT AND WON¿T SIT FLUSH ON THE BONE. THE REAMERS ARE DULLED AND HAVE BURRS . THESE ITEMS WERE PULLED OUT OF THE SETS AND NOT USED IN A CASE. NO SURGICAL DELAY.
Patient problems: No Code Available; No Consequences Or Impact To Patient
MAUDE report 10318346 ↗MalfunctionJul 24, 2020Dull, Blunt; Failure to Cut; Material Deformation; Dull, Blunt; Failure to Cut; Material Deformation
IT WAS REPORTED THAT THE 38 POLY TRIALS ARE DAMAGED WITH SCARS AND MISSING PLASTIC IN AREAS SURGEON AND SPD WANTED THEM REPLACED. PROTECTIVE PLATE IS BENT AND WON¿T SIT FLUSH ON THE BONE. THE REAMERS ARE DULLED AND HAVE BURRS . THESE ITEMS WERE PULLED OUT OF THE SETS AND NOT USED IN A CASE. NO SURGICAL DELAY.
Patient problems: No Code Available; No Consequences Or Impact To Patient
MAUDE report 10318343 ↗MalfunctionJul 10, 2019Dull, Blunt; Material Twisted/Bent; Dull, Blunt; Material Twisted/Bent
IT WAS REPORTED THAT THE REAMER WAS DULL. NEEDS TO BE REPLACED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8775583 ↗
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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