Kirschner wire K10 NS070Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03760225711569), received between Mar 23, 2026 and Mar 25, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 25, 2026Use of Device Problem

  DURING THE PROCEDURE, THE GUIDE PIN BENT AND FRACTURED WHEN REMOVAL WAS ATTEMPTED. A SECOND FRAGMENT REMAINED IN THE PATIENT'S FOOT. NO COMPLICATIONS WERE REPORTED BY THE FACILITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24686329 ↗
• MalfunctionMar 23, 2026Use of Device Problem

  DURING TWO SEPARATE SURGICAL PROCEDURES, A KIRSCHNER WIRE (K-WIRE) BROKE INSIDE THE PATIENT'S TOE DURING USE. THE BROKEN WIRE WAS NOT RETRIEVED OR PRESERVED. LOT NUMBER COULD NOT BE CONFIRMED AND THE PRODUCT EXPIRATION DATE WAS UNAVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24661005 ↗