GLOBAL APG+ 2236-00-021Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295105886), received between Sep 13, 2019 and Mar 30, 2026 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Break” (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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 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 24714555 ↗
• MalfunctionDec 10, 2024Break; Break

  IT WAS REPORTED THAT 52 APG TRIAL WAS BROKEN. EPI BROACH HANDLE BECAME LOOSE. SURGICAL DELAY IS UNKNOWN. NO ADDITIONAL INFORMATION TO REPORT.

  Patient problems: Insufficient Information

  MAUDE report 20895936 ↗
• MalfunctionJul 27, 2021Break; Break

  IT WAS REPORTED THAT THE TRIAL CENTER PEG AND ONE PEG BROKE DURING TRAILING. IT WAS A SIZE 52 TRIAL. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12232565 ↗
• MalfunctionJan 27, 2021Break; Break

  IT WAS REPORTED THAT THE CENTER PEG BROKE WHEN TRIALING. THE PEG WAS REMOVED COMPLETELY FROM THE PATIENT¿S BONE. A SURGICAL DELAY OF 30 SECONDS.

  Patient problems: Insufficient Information

  MAUDE report 11238052 ↗
• MalfunctionMar 17, 2020Break; Display Difficult to Read; Illegible Information; Break; Display Difficult to Read; Illegible Information

  IT WAS REPORTED THAT ONE PEG FROM A 52 APG TRIAL WAS BROKEN OFF OF THE BACK OF THE TRIAL. THEY WAS NOT 100% CONFIDENT IN THE LOT CODE. IT WAS VERY DIFFICULT TO READ.

  Patient problems: Not Applicable

  MAUDE report 9845862 ↗
• MalfunctionSep 13, 2019Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT THE TRIAL HAS EXCESSIVE WEAR DUE TO TRIALING. NOTHING LEFT IN PATIENT AND NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9028110 ↗