Cannulated Screws 71117083Recalls & reported problems
Smith & Nephew, Inc. · 4.0MM DIRECT MEASURING GAUGE F/ 1.3MMX140MM K-WIRE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010173898), received between Sep 9, 2019 and Dec 6, 2020 — classified as 2 malfunctions.
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
- Corroded1
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2020Corroded; Device Markings/Labelling Problem; Corroded; Device Markings/Labelling Problem
IT WAS REPORTED THAT IT WAS NOTICED BY THE HEALTHCARE FACILITY THAT THERE IS RUST ON THE EQUIPMENT AND NUMBERS ARE WEARING OFF. NO CASE OR PATIENT WAS INVOLVED. DEVICE WAS THROWN OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10956136 ↗MalfunctionSep 9, 2019Break; Break
IT WAS REPORTED THAT THE RULER BROKE DURING PROCEDURE. NO INJURIES OR DELAYS REPORTED. BACKUP DEVICE AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8977796 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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