NA 2490-92-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295125938), received between Aug 18, 2017 and Feb 9, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (3 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 9, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT ALL THESE INSTRUMENTS ARE WORN DOWN FROM MANY YEARS OF FREQUENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11305483 ↗
• MalfunctionFeb 9, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT ALL THESE INSTRUMENTS ARE WORN DOWN FROM MANY YEARS OF FREQUENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11305478 ↗
• MalfunctionFeb 9, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT ALL THESE INSTRUMENTS ARE WORN DOWN FROM MANY YEARS OF FREQUENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11305476 ↗
• MalfunctionAug 18, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT THE LCS MILESTONE INSTRUMENTS HAS A LOOSE PLAY ON THE ALIGNMENT TOWER HEAD. THE ROD THEREFORE SWINGS FROM LEFT TO RIGHT AND DOES NOT ACCURATELY DROP DOWN TO CHECK CORRECT ALIGNMENT.

  Patient problems: No Information

  MAUDE report 6804351 ↗