Skip to content

Integra® Miltex® 40-224Recalls & reported problems

Integra Lifesciences Production Corporation · Integra® Miltex® Nail Nipper, Straight Jaws, Double Spring · Class 1

All models of Integra Miltex (21)

Data updated Oct 16, 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 10381780436393), received between Sep 7, 2022 and Sep 7, 2022 — 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 16, 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.

  • MalfunctionSep 7, 2022Break; Break

    A FACILITY REPORTED THAT THE NAIL SPLITTER 4 STR (40-224) HAD A POSSIBLE BROKEN SPRING. IT IS UNKNOWN UNDER WHICH CIRCUMSTANCE THIS MALFUNCTION WAS DISCOVERED; HOWEVER, NO INJURY, DEATH OR SURGICAL DELAY WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15370636 ↗

Other INSTRUMENT, MANUAL, SURGICAL, GENERAL USE devices

All INSTRUMENT, MANUAL, SURGICAL, GENERAL USE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page