DELTA XTEND 2317-70-224Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295532675), received between Feb 21, 2023 and Jun 9, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 9, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE REAMER LOCKED UP AND WOULDN'T SPIN. IT ALSO GOT STUCK ON THE HANDLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17098600 ↗
• MalfunctionFeb 21, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT WHEN PUTTING TOGETHER THE FULL WEDGE AUGMENTED REAMER, THE CONSTRUCT WOULD NOT PROPERLY ENGAGE. THERE WAS A 15-20 MINUTES OF SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16409412 ↗