Peri-Loc 71173623Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010638113), received between Jul 27, 2020 and Jul 27, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Connection 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryJul 27, 2020Connection Problem; Connection Problem

  IT WAS REPORTED THAT DURING TRAUMA SURGERY, WHILE TIGHTENING USING THE 4.7NM TORQUE LIMITER, NO CLICK SOUND FROM THE TORQUE LIMITER AND DIDN'T WORK. THERE WAS NO BACKUP DEVICE AVAILABLE, AND THE PROCEDURE WAS COMPLETED WITH A CHANGE IN SURGICAL TECHNIQUE. THERE WAS A SURGICAL DELAY OF 5 MINUTES, AND NO INJURY TO PATIENT WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10324830 ↗