DELTA XTEND 2407-89-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295285960), received between Jul 29, 2020 and Feb 23, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 23, 2021Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11367259 ↗
• MalfunctionFeb 18, 2021Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11345308 ↗
• MalfunctionFeb 18, 2021Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11345054 ↗
• MalfunctionJul 29, 2020Dull, Blunt; Dull, Blunt

  ADDITIONAL INFORMATION RECEIVED STATED THAT THE EVENT HAPPENED DURING STERILIZATION.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10340879 ↗