NA 128042Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 23596010082514), received between Aug 5, 2024 and Aug 5, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Packaging 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.

• MalfunctionAug 5, 2024Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT A K-WIRE .045X9 2PT DM BOX CONTAINED ALL 6 K-WIRE .062X9 2PT WIRES. NO CASE INVOLVED; THEREFORE, THERE WAS NOT PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19913310 ↗