TITAN™ SZR-0926-030-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10381780258537), received between May 11, 2022 and Dec 9, 2022 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Fracture” (2 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 9, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING SHOULDER SURGERY, THE TIP ON A FIN-LOCK SIZER. S BROKE OUTSIDE OF THE PATIENT ON BACK TABLE. SURGERY WAS RESUMED, WITHOUT ANY DELAY, WITH THE SAME DEVICE. THE PATIENT WAS NOT HARMED AS A CONSEQUENCE OF THIS PROBLEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15948734 ↗
• InjuryJul 6, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING A TKA SURGERY, THE FIN-LOCK SIZER. S BROKE. DOCTOR REMOVE ALL OF THE PIECES THAT FELL INSIDE OF THE PATIENT BY HAND. SURGERY WAS RESUMED, WITHOUT ANY DELAY, WITH A BACK-UP DEVICE. PATIENT WAS NOT HARMED AS CONSEQUENCE OF THIS PROBLEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14933212 ↗
• MalfunctionMay 11, 2022Break; Break

  IT WAS REPORTED THAT FIN-LOCK SIZER. S BROKE IN THE MIDDLE. AS THIS WAS NOTICED AFTER THE PROCEDURE, THE PATIENT WAS NO LONGER INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14352698 ↗