Zimmer® Natural Nail® System 47-2493-211-13Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024298897), received between Sep 7, 2022 and Sep 7, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (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

Recent adverse event reports

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

• MalfunctionSep 7, 2022Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem; Packaging Problem

  IT WAS REPORTED THAT WHEN THE STERILE PACKAGE WAS OPENED BY REMOVING PAPER PEEL, IT WAS OBSERVED GLUE AND PAPER RESIDUE REMAINED ON THE INNER SIDE OF THE PACKAGING. THE SURGERY WAS COMPLETED WITH ANOTHER THE SAME PRODUCT WITH NO HEALTH CONSEQUENCES AND DELAY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED YET.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15368050 ↗