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Symmetry House 61-0380Recalls & reported problems

Aspen Surgical Products, Inc. · Symmetry® Curette, House Stapes, 1.5 mm x 1.8 mm Cup Size, Double-Ended, 6 in, 152 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 00887482113875), received between Dec 10, 2020 and Dec 10, 2020 — classified as 1 malfunction.

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 18, 2026.

Most reported problems

Device problems

  • Break1

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 10, 2020Break

    THE CUSTOMER ALLEGED THAT DURING THE PROCEDURE, THE SURGEON WAS DRILLING WITH A MIDAS REX DRILL. POST DRILLING, THE CURETTE WAS BEING USED IN THE AREA WHEN IT SHEARED. A PIECE OF THE CURRETTE FELL INTO THE PATIENT. THE PIECE WAS REMOVED WITH NO FURTHER AFFECT ON THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10985144 ↗

Other Curette, Ear devices

All Curette, Ear devices →

Sources and updates

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