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Symmetry Kerrison 57-0761Recalls & reported problems

Aspen Surgical Products, Inc. · Symmetry® Kerrison Rongeur, Micro, Thin Footplate, 40° Up, 1 mm, 9 mm Opening, 8 in, 203 mm · Class 1

Data updated Oct 18, 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 00887482093177), received between Nov 25, 2015 and Nov 25, 2015.

The most frequently reported specific device problem is “Missing Value Reason” (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 18, 2026.

Most reported problems

Device problems

  • Missing Value Reason1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • Nov 25, 2015Missing Value Reason

    PART OF A DISTAL TIP BROKE OFF, NO HARM WAS DONE TO THE PATIENT, THEY DIDN'T REPORT ANYTHING ON THEIR END.

    Patient problems: No Code Available

    MAUDE report 5276842 ↗

Other Rongeur devices

All Rongeur devices →

Sources and updates

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