Jet-X 71067327Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010607638), received between Dec 20, 2018 and Dec 20, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (1 report).

1 other recall cover devices cleared under the same FDA submission (K093047); 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. How this data works · Data updated Oct 13, 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.

• MalfunctionDec 20, 2018Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE DRILL AND DRILL SLEEVE JAMMED. NO DELAY TO PROCEDURE, NO INJURY TO PATIENT. DEVICE WILL BE RETURNED. BACKUP USED WAS NOT FROM SMITH AND NEPHEW.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8184248 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K093047. One submission often covers many models, so check the product and lot details in each record.

• Z-0245-2022 · Jun 17, 2021 · Open, Classified
  Ilizarov Wire Tensioner, Model 71070341, UDI (10)08033201842072(10)21HP02550(11)210831(21E434