ANCHORAGE XVIMQ001020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613252267027), received between Jan 26, 2021 and Jan 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult or Delayed Positioning” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 26, 2021Difficult or Delayed Positioning; Difficult to Advance; Difficult or Delayed Positioning; Difficult to Advance

  AS REPORTED: "PRIMARY PROCEDURE, RIGHT FIRST MTP. IT WAS REPORTED THAT WHEN THE DRILL GUIDE WAS SEATED INTO A HOLE OF THE PLATE AND AFTER DRILLING WAS DONE, A THREAD-LIKE PIECE OF METAL WAS SEEN IN THE PATIENT. THE PIECE WAS REMOVED BY THE SURGEON. SURGEON REPORTED THAT IT FELT AS THOUGH THE DRILL GUIDE DID NOT SEEM TO BE SEATING AS DEEPLY IN THE HOLE AS IT HAD IN THE PREVIOUS HOLES, AND BELIEVES THAT THE THREAD OF METAL WAS SHAVED OFF OF THE PLATE WHILE DRILLING. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO DELAY."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11229117 ↗