Scorpio 82-7-0712Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327031041), received between May 17, 2017 and May 17, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult To Position” (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 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.

• MalfunctionMay 17, 2017Difficult To Position; Fitting Problem; Fitting Problem

  SCORPIO KNEE SURGERY: INSERT TIBIAL 7X12MM PS: WHEN TRYING TO PLACE IT AND HIT IT; INSERT NOT ENTERED TO THE TIBIAL TRAY. WIRE WAS OUTSIDE OF ITS ORIGINAL POSITION, AND NOT ALLOWED TO "FALL" IN THE TIBIAL TRAY SO WE HAD TO PUT ANOTHER INSERT LESS THICK.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 6573464 ↗