Skip to content

Zimmer® Natural Nail® System 47-2493-321-11Recalls & reported problems

Zimmer GmbH · ZNN CMN NAIL 11.5MMX32CM 125 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 00889024299290), received between Jan 11, 2019 and Jan 11, 2019 — classified as 1 injury.

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

  • Fracture1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryJan 11, 2019Fracture; Fracture

    PLEASE REFER TO REPORT 0009613350 - 2019 - 00020.

    Patient problems: No Information

    MAUDE report 8238955 ↗

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

All ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices →

Sources and updates

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