LPS 1987-15-217Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295078791), received between Dec 11, 2019 and Dec 11, 2019 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 11, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED TO ADDRESS INCREASING PAIN, DECREASED RANGE OF MOTION, AND LOOSENING OF THE FEMORAL COMPONENT AT THE CEMENT TO IMPLANT INTERFACE.CEMENT MANUFACTURER AND DATE OF IMPLANTATION ARE UNKNOWN. PATELLA WAS WORN AND TIBIAL CONSTRUCT (UNKNOWN PART AND LOT NUMBER) REMAIN INSITU. FEMUR AND PATELLA WERE REVISED. DOI: UNKNOWN; DOR: (B)(6) 2019 LEFT KNEE.

  Patient problems: Limited Mobility Of The Implanted Joint; Pain

  MAUDE report 9451956 ↗