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SMALL CANNULATED SCREWS 71103245SRecalls & reported problems

Smith & Nephew, Inc. · 3.0MM CANNULATED SCREW 45MM STERILE · Class 2 · Implant

All models of SMALL CANNULATED SCREWS (18)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010624000), received between Aug 5, 2021 and Aug 5, 2021 — classified as 1 injury.

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

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.

  • InjuryAug 5, 2021Break; Break

    IT WAS REPORTED THAT, DURING A BIMALLEOLAR OSTEOSYNTHESIS THE HEAD OF A 3.0MM CANNULATED SCREW 45MM WAS SPLIT INSIDE OF THE PATIENT. IT WAS DECIDED TO LEAVE THE BODY OF THE 3.0 MM SCREW INSIDE OF THE BONE OF THE PATIENT, DUE TO IT GAVE A ROTATIONAL STABILITY AND REDUCTION TO THE FRACTURE. SURGERY WAS FINISHED WITHOUT ANY SURGICAL DELAY. PATIENT WAS NOT HARMED AS CONSEQUENCE OF THIS PROBLEM. PATIENT CURRENT HEALTH STATUS IS STABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12285346 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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