VERSANAIL®UNIVERSAL HUMERAL NAIL 1817-08-241Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868021732), received between Sep 1, 2022 and Sep 1, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Unintended Movement” (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.

• InjurySep 1, 2022Unintended Movement; Unintended Movement

  IT WAS REPORTED A PATIENT UNDERWENT A SHOULDER ARTHROPLASTY. SUBSEQUENTLY, PATIENT UNDERWENT REVISION APPROXIMATELY SIX MONTHS POST INITIAL PROCEDURE WHERE THE NAIL WAS REMOVED DUE TO IMPINGEMENT AND SHOULDER PAIN. NO ADDITIONAL PATIENT CONSEQUENCES ARE REPORTED.

  Patient problems: Pain

  MAUDE report 15336096 ↗