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Medline MMSN2014Recalls & reported problems

Medline Industries, Inc. · SCREW,NON-LOCKING,MINI T8,2.0 X 14MM · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489120417), received between Jan 3, 2023 and Jan 31, 2023 — classified as 2 injuries.

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
  • Fracture1

Patient problems

  • Foreign Body In Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 31, 2023Break; Break

    ACCORDING TO THE CUSTOMER, WHEN PERFORMING A "DISTAL BUNION" PROCEDURE ON (B)(6) 2022 THE "SCREW BROKE RIGHT UNDER THE HEAD AND THE THREADS HAD TO BE REMOVED."

    Patient problems: Foreign Body In Patient

    MAUDE report 16274523 ↗
  • InjuryJan 3, 2023Fracture; Fracture

    ACCORDING TO THE CUSTOMER, THERE WAS AN INCIDENT IN THE MIDDLE OF A PROCEDURE WHERE 'THE (2.0MM) NON-LOCKING SCREW HAD TOO MUCH RESISTANCE IN THE DRILL HOLE (1.3MM) RESULTING IN THE HEAD OF THE SCREW BREAKING OFF AT THE SHANK.'

    Patient problems: Foreign Body In Patient

    MAUDE report 16091466 ↗

Other Screw, fixation, bone devices

All Screw, fixation, bone devices →

Sources and updates

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