T2 1830-0720SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540201263), received between Jan 22, 2019 and Jan 22, 2019 — classified as 1 injury.

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

• InjuryJan 22, 2019Break

  IT WAS REPORTED THAT ON (B)(6) 2018, HALF PAST ELEVEN A.M., THE PATIENT¿S RIGHT HUMERUS WAS FRACTURED. WHEN THE DOCTOR PUT HUMERAL NAIL T2 HUMERUS INTO THE PATIENT. THE NEAR LINE OF HUMERAL NAIL T2 WAS BROKEN. THE FRACTURED HUMERAL NAIL WAS TOOK OUT BY THE SURGEON TOOK OUT THE FRACTURED HUMERAL NAIL AND CHANGED A REPLACEMENT. DURING THE REPLACEMENT WAS CONNECTING, THE END LINE OF REPLACEMENT HAS SLIGHT DEFORMATION AND COLOR CHANGED. IT LOOKS TEND TO BE FRACTURE. THIS SURGERY NEED BLOOD TRANSFUSION. THE COMPLAINT ISSUE HAPPENED WHICH LED TO PATIENT NEED MORE BLOOD TRANSFUSION.

  Patient problems: Blood Loss

  MAUDE report 8269511 ↗