DELTA XTEND 2317-70-424Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295532767), received between Apr 11, 2024 and May 28, 2025 — 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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 28, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT DISPOSABLE REAMER HEAD COLD WELLED ONTO THE REAMER SHAFT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22099901 ↗
• MalfunctionDec 9, 2024Break; Break

  IT WAS REPORTED THAT TWO INSTRUMENTS IN THIS CASE MALFUNCTIONED: THE FIRST AUGMENT REAMER HANDLE HAD A BUTTON NEAR THE BACK END WHICH IS SPRING LOADED TO CAPTURE THE HUDSON ADAPTOR CONNECTION. THIS BUTTON WAS STICKING AND REQUIRED THE TECH TO TAP IT ON THE SIDE REPEATEDLY TO SPRING THE BOTTOM UP. THIS SHOULD NOT BE NECESSARY. THE SECOND CENTRAL SCREW, METAGLENE AUGMENTED METAGLENE REAMER HEAD BROKE WHILE REAMING THE GLENOID. THIS LEFT FRAGMENTS IN THE PATIENT WHICH REQUIRED THE SURGEON TO REMOVE.

  Patient problems: Insufficient Information

  MAUDE report 20883131 ↗
• MalfunctionApr 11, 2024Break; Break

  IT WAS REPORTED THAT A PIN BROKE OFF THE WEDGE REAMER. SURGEON REPLACED WITH A NEW PIECE AND IT WORKED FINE. SURGERY WAS DELAYED A 4-5 MINUTES WHILE WE DIAGNOSED THE ISSUE. ALL PIECES WERE RECOVERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19087149 ↗