LPS 1987-27-128Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295079460), received between Feb 7, 2018 and Sep 11, 2024 — classified as 7 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjurySep 11, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT HAD DISLOCATED AND THERE WAS SIGNS OF INFECTION. SO DOCTOR PERFORMED AN I&D AND POLY SWAP AND UPSIZED THE POLY AND PUT A NEW HINGE PIN IN AS WELL. SURGICAL DELAY WAS UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 20193244 ↗
• InjuryFeb 16, 2023Fracture; Fracture

  REVISION COMPLETED FOR INSTABILITY REPORTED DURING PRE-OP DIAGNOSIS. THE LPS INSERT THAT WAS FOUND TO HAVE A DAMAGED TIBIAL POST WAS REMOVED AND REPLACED. THE LPS FEMUR WAS ALSO REMOVED & REPLACED. THERE WAS NO SURGICAL DELAY. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Joint Laxity

  MAUDE report 16386040 ↗
• InjuryJan 4, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT REVISED DUE TO PAINFUL LEFT KNEE. PREVIOUS SURGERY DATE AND LOCATION IS UNKNOWN. NO ADDITIONAL INFORMATION IS AVAILABLE. THERE WAS NO SURGICAL DELAY. DOI: UNKNOWN. DOR: DEC 16, 2022. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Pain

  MAUDE report 16096669 ↗
• InjuryJun 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO KNEE BECAME INFECTED. A WASHOUT/POLY EXCHANGE WERE COMPLETED. DOI: (B)(6) 2021 DOR: (B)(6) 2021 LEFT KNEE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 12040648 ↗
• InjurySep 16, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO PAIN. DOI: (B)(6) 2019, DOR: (B)(6) 2019, RIGHT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 9072661 ↗
• InjurySep 20, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS INFECTION. DOI: UNK. DOR: (B)(6) 2018; UNK KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 7894311 ↗
• InjuryFeb 7, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT WAS REVISED TO ADDRESS PAIN. WASH OUT WITH POLY WAS DONE. DOI: (B)(6) 2017, DOR: (B)(6) 2018, LEFT KNEE.

  Patient problems: Pain

  MAUDE report 7246996 ↗