DELTA XTEND 2307-77-004Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295116233), received between May 7, 2019 and Jun 6, 2022 — 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 6, 2022Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THIS WAS AN RSA FOR TREATING CTA ON (B)(6) 2022. IT WAS VERY TIGHT TO ATTACH THE MODULAR DISK TO A COUNTERPART (UNK ADAPTER). THE PROCEDURE WAS COMPLETED WITHOUT SURGICAL DELAY. THERE WAS NO HARM TO THE PATIENT. THE DEVICE WAS BRAND NEW AND THE FIRST USE WHEN THE ISSUE OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14603614 ↗
• MalfunctionMay 7, 2019Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE SURGEON COULD NOT ATTACHED THE REPORTED DEVICE ON THE ADAPTOR BEFORE THE SURGERY ON UNKNOWN DATE. THEN, THE SURGEON REMOVED THE ADAPTER FROM PROXIMAL REAMING GUIDE AND TRIED TO ATTACH THE REPORTED DEVICE WITH THE ADAPTER, HOWEVER, THE SURGEON COULD NOT ATTACH IT. THE SURGERY WAS PERFORMED AND COMPLETED BY USING ALTERNATIVE DEVISE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8588200 ↗