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V. Mueller NL3785-009Recalls & reported problems

Steris Corporation · RHOTON HOOK ANGLED 90DEG SEMI-SHARP OVERALL LENGTH 7-1/2 inches19.1CM · 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 10885403187124), received between Jan 27, 2021 and Jan 27, 2021 — classified as 1 malfunction.

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

  • Fracture1
  • No Apparent Adverse Event1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • 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.

  • MalfunctionJan 27, 2021Fracture; No Apparent Adverse Event; Fracture; No Apparent Adverse Event

    IT WAS REPORTED THAT THE INSTRUMENT BROKE DURING A CASE. IT WAS REPORTED THAT NO PIECE OF THE DEVICE FELL OFF IN THE PATIENT AND NO MEDICAL INTERVENTION WAS REQUIRED. THE PROCEDURE WAS COMPLETED.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

    MAUDE report 11240135 ↗

Other INSTRUMENT, MICROSURGICAL devices

All INSTRUMENT, MICROSURGICAL devices →

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