LPS 1987-15-315Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295078821), received between Sep 19, 2019 and Apr 25, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Corroded” (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 16, 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.

• InjuryApr 25, 2024Loss of or Failure to Bond; Corroded; Naturally Worn; Loss of or Failure to Bond; Corroded; Naturally Worn

  A DEPUY SYNTHES IMPLANT WAS REVISED AND REVIEWED FOR ANALYSIS REASON FOR REVISION: LOOSE FEMORAL STEM. AT REVISION THE STEM TRUNNION SHOWED FRETTING AND CORROSION. THE BORE OF THE FEMORAL COMPONENT SHOWED FRETTING AND CORROSION.

  Patient problems: Insufficient Information

  MAUDE report 19180366 ↗
• InjurySep 19, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS CHRONIC INFECTION OF A RIGHT DISTAL FEMORAL REPLACEMENT. THIS IS ALL THE INFORMATION THAT IS AVAILABLE. DOI: (B)(6) 2016; DOR: (B)(6) 2019; RIGHT KNEE.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 9088513 ↗