Peri-Loc 71173616Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010637178), received between Feb 14, 2021 and Feb 24, 2022 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 24, 2022Break; Break

  IT WAS REPORTED THAT, DURING TOTAL HIP REPLACEMENT, THE TIP OF A T25 SELF-RET SCREWDRIVER W/QC 178 MM BROKE OFF INSIDE THE PATIENT. ALL PIECES WERE RECOVERED. SURGERY WAS RESUMED, WITHOUT ANY DELAY, WITH A SMITH & NEPHEW BACK-UP DEVICE. PATIENT WAS NOT INJURED AS CONSEQUENCE OF THIS PROBLEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13591603 ↗
• MalfunctionApr 6, 2021Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE LARGE SCREWDRIVER HANDLE ((B))4)) AND THE T25 SELF-RET SCREWDRIVER W/QC 178MM ((B)(4)) ARE STRIPPED AND DO NOT STAY TIGHT. THE FAILURE WAS NOTICED DURING SET UP OR INSPECTION. THE PROCEDURE WAS COMPLETED USING A SN BACKUP DEVICE. NO SURGICAL DELAY OR INJURY TO THE PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11624944 ↗
• MalfunctionFeb 14, 2021Mechanical Jam; Separation Problem; Mechanical Jam; Separation Problem

  IT WAS REPORTED THAT, IT IS NOT POSSIBLE TO SEPARATE A T25 SELF-RET SCREWDRIVER W/QC 178MM FROM THE HANDLE. IT IS UNKNOWN WHETHER THE EVENT HAPPENED AND IF THERE WAS A PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11326213 ↗