Acute QC Strut and Components 71935869Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556807088), received between Oct 23, 2025 and Oct 23, 2025 — classified as 1 malfunction.

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

• MalfunctionOct 23, 2025Fracture; Fracture

  IT WAS REPORTED THAT, DURING AN ANKLE SPANNING PROCEDURE, THREE (3) ACUTE QC STRUT LONG BROKE WHEN THEY WERE BEING TIGHTENED. THE PROCEDURE WAS RESUMED AFTER A DELAY GREATER THAN 30 MIN. HOWEVER, IT IS UNKNOWN HOW THE PROCEDURE WAS FINISHED. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23364556 ↗