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SMALL CANNULATED SCREWS 71103228SRecalls & reported problems

Smith & Nephew, Inc. · 3.0MM CANNULATED SCREW 28MM STERILE · Class 2 · Implant

All models of SMALL CANNULATED SCREWS (18)

Data updated Oct 16, 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 03596010623928), received between Apr 5, 2021 and Apr 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 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.

  • InjuryApr 5, 2021Break; Break

    IT WAS REPORTED THAT, DURING A CANNULATED SCREW PROCEDURE, SURGEON WAS FINISHING PLACING THE SCREW WHEN HE FELT/HEARD A SNAP. THE HEAD OF THE SCREW HAD COME OFF AND FELL ON THE FLOOR. THE SHAFT OF THE SCREW WAS FIXED INTO THE BONE AND NO PART WAS STICKING OUT OF THE BONE. THE SCREW WAS LEFT IN THE BONE. THE HEAD OF THE SCREW WAS DISCARDED. INSTRUMENTS WERE INSIDE THE PATIENT. PROCEDURE WAS COMPLETED WITH THE SAME DEVICE. THERE WAS NO DELAY OR FURTHER COMPLICATIONS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11612133 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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