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Peri-Loc 71173612Recalls & reported problems

Smith & Nephew, Inc. · T20 REMOVAL SCREWDRIVER SHAFT W/QUICK CONNECT 178MM · Class 1

All models of Peri-Loc (102)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010637277), received between Mar 30, 2021 and Mar 30, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incomplete or Inadequate Connection” (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

Device problems

  • Incomplete or Inadequate Connection1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 30, 2021Incomplete or Inadequate Connection; Incomplete or Inadequate Connection

    IT WAS REPORTED THAT DURING A PERILOC L-P TIBIA PLATE REMOVAL, THE DR REMOVED PLATE AND SCREWS FOR A PATIENT THAT HEALED. ORIGINAL SURGERY WAS IN 2015 AT ST JOSEPH REGIONAL MEDICAL CENTER. DURING THE CASE THE SCREWDRIVER BECAME STUCK IN THE SCREWDRIVER HANDLE. THE CASE WAS COMPLETED AS EXPECTED AND NO FURTHER COMPLICATIONS WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11593486 ↗

Other SCREWDRIVER devices

All SCREWDRIVER devices →

Sources and updates

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