LPS 1987-11-205Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295078654), received between Dec 13, 2017 and Feb 5, 2025 — classified as 3 injuries.

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

• InjuryFeb 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT CONTINUES TO HAVE RECURRENT INFECTIONS AND INFLAMMATION AROUND PATIENT'S PROSTHESIS EVEN AFTER MULTIPLE 2 STAGE REVISIONS. THE QUESTION HAS BEEN RAISED AS TO WHETHER PATIENT IS HAVING A REACTION TO THE METAL. THEREFORE ALLERGY TESTING IS GETTING DONE FOR PATIENT BUT FOR THAT PATIENT NEEDS TO KNOW THE EXACT COMPOSITION OF IMPLANTS SO DERMATOLOGY KNOW WHAT TO TEST FOR.

  Patient problems: Inflammation; Unspecified Infection

  MAUDE report 21314299 ↗
• InjuryJan 18, 2019Loss of Osseointegration; Loss of Osseointegration

  IT WAS REPORTED THAT THE PATIENT HAD FELL AND ALL THE COMPONENTS CAME LOOSE. THERE WAS LOOSENING OF THE FEMUR AT BONE TO IMPLANT INTERFACE.

  Patient problems: Inadequate Osseointegration; No Code Available

  MAUDE report 8261103 ↗
• InjuryDec 13, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated

  WHEN DR (B)(6) WAS REVISING A RIGHT HIP DISLOCATION IT WAS DISCOVERED THAT THE PROXIMAL BODY WAS A LEFT TROCHANTER BODY 15 DEGREE REF NUMBER 1987-11-205 IN A RIGHT HIP. ADDITIONALLY DUE TO THE DISLOCATION HE REPLACED THE CONSTRAINED ACETABULAR LINER AND THE FEMORAL HEAD PATIENT CONSEQUENCE? :NO. ACTION TAKEN FOR PROCEDURE:REPLACED THE LEFT WITH A RIGHT TROCHANTERIC BODY AND A NEW ACETABULAR LINER BI POLAR HEAD AND A ARTICULEZE FEMORAL HEAD IS THE INFORMATION BEING SUBMITTED FOR THIS COMPLAINT ALL THE DETAILS THAT ARE KNOWN/AVAILABLE REGARDING THIS EVENT? : YES.

  Patient problems: Joint Dislocation

  MAUDE report 7113336 ↗