GLOBAL AP 2130-01-060Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP CALCAR REAMER 40/44 SMALL · Class 1
All models of GLOBAL AP (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295090557), received between Feb 22, 2023 and Feb 22, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).
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
- Device-Device Incompatibility1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 22, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT A SMALL CALCAR REAMER FROM GLOBAL AP CORE INSTRUMENTS NEEDS TO BE DISCARDED. THE REAMER BECAME STUCK OVER THE CALCAR ALIGNMENT GUIDE ASSEMBLY. THE INSTRUMENTS WERE TESTED THE LARGE REAMER AND IT IS DEFINITELY THE SMALL CALCAR REAMER WHICH IS MISSHAPEN NOT THE ALIGNMENT GUIDE ASSEMBLY. ALTHOUGH THE ALIGNMENT GUIDE NOW LOOKS DAMAGED. WAS ABLE TO BE REMOVED FROM THE PATIENT WITH EASE AND REQUIRED SOME EXTRA WORK ON THE BACK TABLE TO SEPARATE THE 2 INSTRUMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16416772 ↗
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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