LPS 1987-25-111Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295079156), received between Sep 22, 2021 and Mar 13, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryMar 13, 2026Fracture

  ADDITIONAL INFORMATION RECEIVED: WAS THERE ANY REVISION SURGERY PERFORMED? IT WAS PLANNED ON (B)(6) 2026.

  Patient problems: Insufficient Information

  MAUDE report 24590754 ↗
• InjurySep 19, 2024Loss of or Failure to Bond; Loss of or Failure to Bond

  PATIENT WAS REVISED DUE TO LOOSENING OF LPS STEM AT CEMENT TO IMPLANT INTERFACE. CEMENT MANUFACTURER WAS UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2024, AFFECTED SIDE: LEFT KNEE.

  Patient problems: Insufficient Information

  MAUDE report 20263669 ↗
• InjuryMay 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED: WAS THERE ANY SURGICAL DELAY RELATED TO THE EVENT? IF YES, WHAT IS THE DURATION OF THE DELAY? NO. WAS THERE ANY PATIENT HARM/CONSEQUENCE RELATED TO THE EVENT? NO.

  Patient problems: Joint Laxity; Physical Asymmetry

  MAUDE report 19286562 ↗
• InjuryNov 14, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT PRESENTED WITH AN INFECTED JOINT REPLACEMENT. AN IRRIGATION AND DEBRIDEMENT (I&D) WAS PERFORMED WITH PLANNED EXCHANGE OF MODULAR COMPONENTS AND PLACEMENT OF RESORBABLE ANTIBIOTIC BEADS. STEM WAS IMPLANTED ON (B)(6) 2023. FEMUR SEGMENT AND INSERT WERE EXCHANGED ON (B)(6) 2023 POST FALL AND DEHISCENCE OF INCISION. NO PATIENT HARM OCCURRED. NO DELAY WAS EXPERIENCED. IN AN EFFORT TO REMOVE THE SEGMENT OF AN DISTAL FEMUR, THE CEMENTED STEM WAS ALSO REMOVED. NEW COMPONENTS WERE IMPLANTED UNEVENTFULLY. DOI: (B)(6) 2023; DOI(STEM): (B)(6) 2023; DOR: (B)(6) 2023; AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 18132334 ↗
• InjuryAug 9, 2022Loss of or Failure to Bond; Loss of or Failure to Bond

  PATIENT WAS REVISED DUE TO PERIPROSTHETIC FRACTURE AND LOOSENING OF THE CEMENTED STEM AT THE BONE TO CEMENT AND CEMENT TO IMPLANT INTERFACES. COMPETITOR CEMENT WAS USED. DOI: (B)(6) 2019. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Limb Fracture

  MAUDE report 15191740 ↗
• InjurySep 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION LPS FOR PATELLA SCARRING/ CLUNKING AND PAIN - APPEARED TO BE TISSUE RUBBING ON POROUS COLLAR ON LPS STEM. LPS REMOVED AND LPS WITH SLEEVE PUT IN. DOI: UNKNOWN. DOR: (B)(6) 2021, UNKNOWN SIDE.

  Patient problems: Pain; Scar Tissue

  MAUDE report 12513044 ↗