GLOBAL APG+ 2236-00-017Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ GLENOID GRASPER · 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 10603295105848), received between Oct 17, 2018 and Mar 30, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break2
- Inadequacy of Device Shape and/or Size1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- Not Applicable1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 30, 2026Break
IT WAS REPORTED THAT TRIAL APG SIZE 52 BROKE DURING TRIALING AND ONE PERIPHERAL PEG BROKE OFF. ALL PIECES WERE RECOVERED. NO DELAY TO SURGERY OCCURRED. THE PHYSICIAN STATES THE GLENOID GRASPER WAS LOOSE. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24714548 ↗MalfunctionDec 3, 2024Break; Break
IT WAS REPORTED THAT THE AGP GRASPER WAS BROKEN.
Patient problems: Insufficient Information
MAUDE report 20835566 ↗MalfunctionOct 17, 2018Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
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- MEDLINE DYNJ04048Medline Industries, Inc. · FORCEPS, GENERAL & PLASTIC SURGERY2 recalls0 reports
- Sklar Instruments 96-2549Sklar Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion I68420Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion 66440Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 66195Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 67310Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
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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