Tornier Humeral Nail 7020140Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00846832004775), received between Aug 21, 2023 and Aug 21, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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.

• MalfunctionAug 21, 2023Component Missing; Inaccurate Information; Component Missing; Inaccurate Information

  IT WAS REPORTED THAT WHEN THE BOX WAS OPENED IT CONTAINED A MARKER WIRE AND NOT THE DRILL BIT THAT THE BOX WAS LABELED FOR.

  Patient problems: Insufficient Information

  MAUDE report 17590071 ↗