RADIOLUCENT TARGETING ARM, TROCHANTERIC NAIL 125° 1267Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848665010879), received between Sep 25, 2023 and Sep 25, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective 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.

• MalfunctionSep 25, 2023Defective Device; Defective Device

  ON 08/28/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS-06016727 THAT A 1267-000 TARGETING ARMS DISTAL HOLE ON THE JIG WAS NOT LINING UP ON THE SHORT NAIL. THIS OCCURRED DURING A HIP ORIF, WHERE THE DRILL WAS SKIVING ANTERIORLY. THERE WAS NO PATIENT EFFECT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17810308 ↗