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Symmetry Surgical 90-4012Recalls & reported problems

Aspen Surgical Products, Inc. · Symmetry® Monopolar Electrode; L Hook w/Valve; Fully Insulated; 5 mm Shaft; 12 1/2 in · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887482129708), received between Aug 14, 2020 and Aug 14, 2020 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Burn, Thermal1

Recent adverse event reports

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

  • InjuryAug 14, 2020Adverse Event Without Identified Device or Use Problem

    DURING A PROCEDURE THE MONOPOLAR ELECTRODE BURNT THE PATIENT'S LIVER.

    Patient problems: Burn, Thermal

    MAUDE report 10411384 ↗

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Sources and updates

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