Scorpio 82-6-0912Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327030693), received between May 23, 2019 and May 23, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Osseointegration Problem” (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.

• InjuryMay 23, 2019Osseointegration Problem; Osseointegration Problem

  REVIEW OF SUMMARY REPORT SUBMITTED AS PART OF AN IIS MILESTONE REVEALED FRK063 WAS REVISED DUE TO OSTEOLYSIS AND LOOSENING. ASEPTIC LOOSENING OF THE FEMORAL COMPONENT DUE TO OSTEOLYSIS. RIGHT TOTAL KNEE REVISION ARTHROPLASTY, FEMORAL COMPONENT AND TIBIAL LINER INSERT EXCHANGE WITH SYNOVECTOMY AND BONE GRAFTING OF A CONTAINED MEDIAL FEMORAL CONDYLAR DEFECT PERFORMED (B)(6) 2014. COMPONENTS USED IN REVISION: SCORPIO NRG #9 FEMUR WITH SIMPLEX P CEMENT AND 9X15 CR INSERT.

  Patient problems: Inadequate Osseointegration; Injury; Osteolysis

  MAUDE report 8636019 ↗