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Cannulated Screws 71120006Recalls & reported problems

Smith & Nephew, Inc. · WASHER 8MM Outer Diameter 4MM Inner Diameter · Class 2

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 03596010174338), received between Jun 30, 2020 and Jun 30, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Expiration Date Error” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Expiration Date Error1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 30, 2020Expiration Date Error; Adverse Event Without Identified Device or Use Problem; Expiration Date Error; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT AFTER SURGERY THE CIRCULATOR NOTICED THAT THE IMPLANT STICKER SHOWS THAT THE IMPLANT WAS EXPIRED. THE IMPLANT STILL REMAINS INSIDE THE PATIENT. THE PATIENT OUTCOME IS UNKNOWN.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Information

    MAUDE report 10215886 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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