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V. Mueller GL1625Recalls & reported problems

Steris Corporation · V. Mueller HUNTER LARGE UTERINE CURETTE BLADE 3CM WIDE WORKING LENGTH 8 inches 20.3CM OVERALL LENGTH 12-3/4 inches 32.4CM · Class 1

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 10885403044748), received between Nov 19, 2020 and Nov 19, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Material Integrity Problem1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionNov 19, 2020Material Integrity Problem; Material Integrity Problem

    IT WAS REPORTED THAT THE INSTRUMENT CAME APART DURING PROCEDURE AND HAD TO BE RETRIEVED BY THE SURGEON.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10870942 ↗

Other CURETTE, UTERINE devices

All CURETTE, UTERINE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.