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ILIZAROV SYSTEMS 103000Recalls & reported problems

Smith & Nephew, Inc. · TUBULAR ANGULATED WRENCH 10MM · Class 1

All models of ILIZAROV SYSTEMS (3)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010031884), received between May 11, 2021 and May 11, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Corroded” (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

  • Corroded1

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.

  • MalfunctionMay 11, 2021Corroded; Corroded

    IT WAS REPORTED THAT, A RATCHET WRENCH WAS SEEN TO STICK, A UNIVERSAL CHUCK DID NOT TIGHTEN PROPERLY, A TUBULAR ANGULATED WRENCH WAS RUSTY, A DRILL TISSUE PROTECTOR - LONG AND A DEPTH GAUGE SHORT WERE BENT. AS THIS WAS NOTICE IN A FIELD INSPECTION, NOT PATIENT WAS INVOLVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11806441 ↗

Other WRENCH devices

All WRENCH devices →

Sources and updates

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