LPS 2987-15-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295157854), received between Jul 23, 2021 and Nov 15, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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.

• MalfunctionNov 15, 2021Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT THE PIN HAS A BURR AND WOULD NOT SEAT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12813390 ↗
• MalfunctionJul 23, 2021Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON (B)(6) 2021 SURGEON WAS PUTTING AN LPS DISTAL FEMUR TRAIL TOGETHER. HE USED A X-SM RIGHT DISTAL FEMUR TRIAL AND A X-SM HINGE PIN AND NOTICED THAT THE HINGE PIN WAS HAVING A DIFFICULT TIME PASSING THROUGH THE FEMUR. AFTER FURTHER INSPECTION AFTER THE CASE, BOTH THE HINGE PIN AND INNER PART OF THE FEMUR ARE DAMAGED AND NEED TO BE REPLACED. THERE WERE NO BROKEN PIECES AND ALL COMPONENTS WERE FULLY INTACT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12221062 ↗