LCS MILESTONE 2287-55-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295110293), received between Jan 25, 2018 and Jan 29, 2019 — 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. 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.

• MalfunctionJan 29, 2019Material Deformation; Material Twisted/Bent; Material Deformation; Material Twisted/Bent

  THE (B)(6) ENGINEERING ASSESSMENT TEAM DOCUMENTED AND ATTACHED PHOTOGRAPHS OF THE DEVICE IDENTIFYING THE GUIDE WAS CRACKED AND THERE WAS EXTENSIVE/HEAVY IMPACTION DAMAGE COVERING THE SURFACE OF THE FINISHING GUIDE. THE LOT I/D AH0102 (JAN 2002) MAKES THIS INSTRUMENT APPROX. 16+YRS OLD.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8285310 ↗
• MalfunctionJan 25, 2018Material Deformation; Appropriate Device Problem Term/Code Not Available; Material Deformation; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT THE CUTTING BLOCK SPRUNG. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7218514 ↗