M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System 03.65.704Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030881084), received between Feb 5, 2021 and Feb 5, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Malposition of Device” (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.

• InjuryFeb 5, 2021Malposition of Device

  REVISION SURGERY 1 MONTH AFTER PRIMARY SURGERY FOR SCREW MALPOSITIONING. THE SCREW WAS IMPLANTED 2MM TOO DEEP INTO THE BONE DURING THE PRIMARY LEAD TO CONTACT WITH NERVE ROOT L5. DURING REVISION, THE SCREW CAME OUT VERY EASILY, BUT THE WASHER NEEDED SEVERAL EXTRACTION ATTEMPTS TO BE REVISED. FINALLY REMOVED USING FORCEPS.

  Patient problems: Insufficient Information

  MAUDE report 11284922 ↗