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Zimmer® Natural Nail® System 47-2493-343-10Recalls & reported problems

Zimmer GmbH · ZNN CMN NAIL 10MMX34CM 130 L · Class 2 · Implant

All models of Zimmer Natural Nail System (57)

Data updated Oct 18, 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 00889024299528), received between Oct 3, 2022 and Oct 3, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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

  • Migration or Expulsion of Device1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryOct 3, 2022Migration or Expulsion of Device; Migration or Expulsion of Device

    IT WAS REPORTED THAT A PATIENT UNDERWENT A PROCEDURE TO REPAIR A LEFT, COMMINUTED, SUBTROCHANTERIC FRACTURE. ON AN UNKNOWN TIMEFRAME POST-IMPLANTATION, THE CONNECTION BETWEEN THE TITANIUM ROD OF THE FEMUR AND THE SCREW SPINDLE OF THE JOINT HEAD LOOSENED AND SHIFTED. THE FRACTURE HAS NOT HEALED DUE TO THE LOOSENING AND CONSTANT MOVEMENTS. ADDITIONAL SURGERY IS PENDING. DUE DILIGENCE IS IN PROGRESS FOR THIS EVENT; TO DATE NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Patient problems: Failure of Implant

    MAUDE report 15526761 ↗

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

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Sources and updates

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