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PENDING MMPF1110Recalls & reported problems

Medline Industries, Inc. · PIN, TEMP FIX, SMOOTH MINI, 1.1 X 10MM · 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 10888277690875), received between Sep 22, 2020 and Sep 22, 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. How this data works · Data updated Oct 13, 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 22, 2020Break; Break

    IT WAS REPORTED THAT THE WIRES BROKE WHILE BEING SECURED. THE ENDS OF THE BROKEN WIRES REMAIN IN THE PATIENT'S FOOT DUE TO THE BENEFIT OUTWEIGHING THE RISK OF REMOVAL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10568003 ↗

Other BENDER devices

All BENDER devices →

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