TRIAX 5150-3-075Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327072839), received between Dec 19, 2016 and Dec 19, 2016 — classified as 2 injuries.

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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 19, 2016Adverse Event Without Identified Device or Use Problem

  IT HAS BEEN REPORTED THAT ON THE (B)(6), THE SURGEON IMPLANTED 2 PIN CLAMP IN AN PATIENT WITH ACHONDROPLASIA, IN ORDER TO MAKE A FEMUR BILATERAL ENLARGEMENT. THIS WAS A SECOND PROCEDURE.

  Patient problems: No Code Available

  MAUDE report 6185342 ↗
• InjuryDec 19, 2016Adverse Event Without Identified Device or Use Problem

  IT HAS BEEN REPORTED THAT ON THE 14TH OCTOBER, THE SURGEON IMPLANTED 2 PIN CLAMP IN AN PATIENT WITH ACHONDROPLASIA, IN ORDER TO MAKE A FEMUR BILATERAL ENLARGEMENT. THIS WAS A SECOND PROCEDURE.

  Patient problems: No Code Available

  MAUDE report 6185273 ↗