LCS MILESTONE 2287-35-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295110101), received between Jul 13, 2017 and Sep 18, 2020 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (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 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.

• MalfunctionSep 18, 2020Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT THE FIXATION PIN GOT STUCK INSIDE AP BLOCK. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10555544 ↗
• MalfunctionJan 10, 2020Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT THE INSTRUMENT WAS WARPED IN HOLE. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9577236 ↗
• MalfunctionOct 23, 2018Break; Break

  IT WAS REPORTED THAT THE HANDLE BROKE OFF.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7994760 ↗
• MalfunctionJul 13, 2017Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE LCS LARGE HIP BLOCK HAS A BURR IN THE HOLE. DRILL WILL NOT GO THROUGH THE HOLE SMOOTHLY.

  Patient problems: No Information

  MAUDE report 6710168 ↗