Tornier Humeral Nail 0020600Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00846832091072), received between Mar 20, 2023 and Mar 20, 2023 — classified as 1 injury.

2 other recalls cover devices cleared under the same FDA submission (K082754, K230352); they may or may not involve this specific model.

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.

• InjuryMar 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO FRACTURE DISPLACEMENT 7 DAYS POST-OP.

  Patient problems: Bone Fracture(s)

  MAUDE report 16577070 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082754, K230352. One submission often covers many models, so check the product and lot details in each record.

• Z-1757-2018 · Mar 26, 2018 · Terminated
  AEQUALIS HUMERAL NAIL DRILL BIT, REF 7020140 Product Usage: The Aequalis Humeral Nail system is intended to provide temporary stabilization of various types of proximal and/or di
• Z-2315-2015 · Jun 25, 2015 · Terminated
  Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.