DELTA XTEND 2317-70-013Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295532507), received between Mar 2, 2026 and Mar 4, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionMar 4, 2026Break; Material Deformation; Unintended Movement

  IT WAS REPORTED THAT THE INNER SHAFT WAS BENT AND WOBBLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24505478 ↗
• MalfunctionMar 2, 2026Material Deformation; Unintended Movement

  IT WAS REPORTED THAT THE INNER SHAFT IS BENT AND MADE OUTER SHAFT WOBBLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24491409 ↗