NA 329.142Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887587039183), received between Jul 25, 2024 and Jul 25, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical 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. How this data works · Data updated Oct 13, 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.

• MalfunctionJul 25, 2024Mechanical Problem; Mechanical Problem

  IT WAS REPORTED DURING A PROCEDURE ON (B)(6) 2024, IN THE BENDING IRON, A PART KEEPS FALLING OUT OF THE INSTRUMENT. THERE WAS NO IMPACT ON THE PROCEDURE OR THE PATIENT. THIS REPORT IS FOR ONE BENDING PLIERS FOR PLATES 1.5 TO 2.7, LENGTH 140 MM. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: Insufficient Information

  MAUDE report 19826350 ↗