LCS 2267-26-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295108757), received between Feb 7, 2019 and Feb 7, 2019 — classified as 3 malfunctions.

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

• MalfunctionFeb 7, 2019Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem; Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem

  FEMORAL GUIDE POSITIONER IS TOO SHORT IN COMPARISON TO THE SPACER SHIM AND FOR THIS REASON THE INSTRUMENT IS NOT FIT FOR USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8316638 ↗
• MalfunctionFeb 7, 2019Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem; Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem

  THE FEMORAL GUIDE POSITIONER IS TOO SHORT IN COMPARISON TO THE SPACER SHIM AND FOR THIS REASON THE INSTRUMENT IS NOT FIT FOR USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8316612 ↗
• MalfunctionFeb 7, 2019Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem; Inadequacy of Device Shape and/or Size; Fitting Problem; Connection Problem

  THE FEMORAL GUIDE POSITIONER IS TOO SHORT IN COMPARISON TO THE SPACER SHIM AND FOR THIS REASON THE INSTRUMENT IS NOT FIT FOR USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8315715 ↗