LPS 1987-15-215Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295078777), received between Jun 16, 2020 and Jun 16, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 16, 2020Loss of or Failure to Bond; Loss of or Failure to Bond

  REVISION TOTAL KNEE REPLACEMENT. PATIENT HAS HAD MANY REVISIONS FOR INFECTION. THE MOST RECENT 3.5 YEARS AGO WHICH IS BEING REVISED FOR LOOSENING (CEMENT BONE INTERFACE PREDOMINANTLY) OF LPS FEMORAL CEMENTED STEM. CEMENTED LPS FEMORAL STEM LOOSE. SALVAGE PROCEDURE TO CEMENT ANOTHER LONGER STEM INSITU. TIBIAL COMPONENTS REMAINS INSITU. TIBIAL BEARING EXCHANGED. RELEVANT PATIENT PRE-EXISTING CONDITIONS/ COMORBIDITIES; HISTORY OF INFECTION MULTIPLE REVISION TOTAL KNEES FOR SAME. VARIOUS PROSTHESIS AND TREATING SURGEONS. MALE PATIENT (B)(6). NOTE: MULTIPLE REVISIONS FOR INFECTION OF RIGHT TOTAL KNEE PROSTHESIS. MOST RECENT SURGERY DATE UNKNOWN HOWEVER OVER 3 YEARS AGO AND THIS MAY NOT BE ON FILE AS A PRODUCT COMPLAINT AS IT MAY NOT HAVE BEEN A DEPUY SYNTHES PROSTHESIS THAT WAS REVISED AT THE TIME. SUPPORTING DATA: NOTHING FURTHER AVAILABLE.

  Patient problems: Injury; No Code Available; Unspecified Infection

  MAUDE report 10158022 ↗