T2 1829-1174SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613153297482), received between Aug 6, 2019 and Aug 6, 2019 — classified as 1 injury.

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.

• InjuryAug 6, 2019Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT'S RIGHT KNEE WAS REVISED IN (B)(6) 2018 WITH THE REMOVAL OF A SCREW FROM A T2 NAIL. IN (B)(6) 2019, SURGEON PRONOUNCED PATIENT AS 70% HEALED (RANGE-OF-MOTION ISSUES) AND NOTHING FURTHER COULD BE DONE. PATIENT CONTINUES TO NEED CRUTCHES TO AMBULATE.

  Patient problems: Ambulation or Postural Difficulties; Loss of Range of Motion; Nonunion/Delayed-union Bone Fracture

  MAUDE report 8867746 ↗