Skip to content

TENXOR 4936-2-040Recalls & reported problems

Stryker GmbH · Wire Post · Class 2

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 07613327095210), received between Sep 17, 2018 and Sep 17, 2018 — classified as 1 malfunction.

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 Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionSep 17, 2018Break

    TENXOR WIRE CLAMP BROKE INTO PIECES AT END OF PROCEDURE, IDENTIFIED AT THE END OF CASE AFTER TENSIONING WIRES AND CUTTING AND BENDING THEM OVER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7883245 ↗

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE devices

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page