GLOBAL APG+ 2236-10-008Recalls & reported problems

Summary

The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 10603295106050), received between Dec 20, 2018 and Jul 27, 2026 — classified as 12 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (8 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 12 most recent of 12 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 27, 2026Material Deformation

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50038093 ↗
• MalfunctionApr 10, 2024Failure to Cut; Scratched Material; Failure to Cut; Scratched Material

  BLUNT REAMER, THERE WAS A 1 MINUTE SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19081943 ↗
• MalfunctionApr 9, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMER WAS FOUND TOO BE BLUNT. NO IMPACT ON SURGERY NOR PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19072255 ↗
• MalfunctionOct 26, 2023Failure to Cut; Failure to Cut

  REAMER IS GETTING DULL AND WAS NOT ABLE TO REAM BONE. TO COMPLETE THE CASE, A DIFFERENT TRAY WAS OPENED. NO DELAY OR PATIENT CONSEQUENCES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18014156 ↗
• MalfunctionApr 5, 2023Failure to Cut; Failure to Cut

  IT WAS REPORTED REAMER WASN'T SHARP ENOUGH TO GET THROUGH THE TOUGH BONE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16683894 ↗
• MalfunctionMar 23, 2022Failure to Cut; Failure to Cut

  GLENOID STEP DRILL AND GLENOID REAMER BLUNT OUT OF CONSIGNMENT SET- NOTED IN CASE TODAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13869263 ↗
• MalfunctionSep 22, 2021Failure to Cut; Failure to Cut

  GLENOID REAMER USED FROM MURDOCH'S CONSIGNMENT SET DURING A CASE WAS BLUNT - SURGEON STRUGGLED TO ACHIEVE DESIRED GLENOID REAMING AS A RESULT. SURGEON EVENTUALLY ACHIEVED SUFFICIENT REAMING. THERE WAS A ONE MINUTE SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12513543 ↗
• MalfunctionJun 18, 2021Failure to Cut; Failure to Cut

  SURGEON COMPLAINED THAT GLENOID REAMER FROM DELTA XTEND SET WAS BLUNT. NO SURGICAL DELAYS REPORTED. PROCEDURE WAS SUCCESSFULLY COMPLETED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12025558 ↗
• MalfunctionMay 26, 2021Failure to Cut; Failure to Cut

  THE ACCESS REAMER SIZE 40 IS BLUNT AND NEEDS TO BE REPLACED OR SHARPENED, SURGERY DELAY 5 MINUTES. NO PATIENT CONSEQUENCES.

  Patient problems: Insufficient Information

  MAUDE report 11891696 ↗
• MalfunctionMar 30, 2021Material Deformation; Material Deformation

  BENT INSTRUMENTS BEING REPORTED. SURGICAL DELAY MAX 1 MINUTE.

  Patient problems: Insufficient Information

  MAUDE report 11589010 ↗
• MalfunctionDec 28, 2018Dull, Blunt; Dull, Blunt

  WHILE PERFORMING A DELTA XTEND CASE, THE GLENOID REAMER APPEARED TO BE BLUNT AND SURGEON STRUGGLED TO REAM THE GLENOID EFFICIENTLY. NO INTERRUPTION TO THE PROCEDURE, BUT NEEDS REPLACING FOR FURTHER CASES. NO AE TO PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8204136 ↗
• MalfunctionDec 20, 2018Dull, Blunt; Dull, Blunt

  SURGEON REPORTED REAMER WAS BLUNT AFTER THE CASE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8186466 ↗