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EVOS 71175064Recalls & reported problems

Smith & Nephew, Inc. · EVOS SMALL FRAGMENT PLATE BENDING PLIERS · Class 1

All models of EVOS (190)

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 00885556635957), received between Dec 30, 2020 and Dec 30, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Corroded” (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

  • Corroded1

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.

  • MalfunctionDec 30, 2020Corroded; Corroded

    IT WAS REPORTED THAT IN A EVOS SMALL FRAGMENT PLATE BENDING PLIERS, PLIERS ARE STARTING TO RUST. NO CASE INVOLVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11095307 ↗

Other INSTRUMENT, BENDING OR CONTOURING devices

All INSTRUMENT, BENDING OR CONTOURING devices →

Sources and updates

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