TOMOFIX 440.885Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982220790), received between Jul 9, 2018 and Jul 9, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical Problem” (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 16, 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.

• InjuryJul 9, 2018Mechanical Problem; Mechanical Problem

  (B)(6) REPORTS THAT DURING REMOVAL OF TOMOFIX LATERAL DISTAL FEMUR PLATE ON AN UNKNOWN DATE, THE SURGEON DESCRIBED THE SCREW AND PLATE JUNCTION STATUS AS ¿COLD WELDING¿. THE SURGEON HAD TROUBLE REMOVING THE TITANIUM TOMOFIX PLATE BECAUSE THE UNKNOWN SCREWS STRONGLY ADHERED TO THE PLATE. THE SURGEON ALWAYS FINISHED THE LAST SCREW INSERTION THREADS USING A TORQUE LIMITING SCREWDRIVER AS DESCRIBE AND PROPOSED IN THE TECHNIQUE GUIDE. DURING THE REMOVAL, THE SURGEON HAD TO USE A BROKEN SCREW REMOVAL SET AND DIAMOND BURR TO SHEAR OFF THE SCREW HEAD AT THE PLATE JUNCTION TO ENABLE REMOVAL OF THE PLATE AND SCREW CONSTRUCT. THE SURGEON ADDED THAT THE PLATE ALWAYS ACHIEVED CLINICAL RESULT GOAL BUT THE CONSTRUCT IS A NIGHTMARE TO REMOVE AFTER BONE HEALING. IT WAS UNKNOWN IF THERE WAS A SURGICAL DELAY RELATED TO THE EVENT. THERE WAS NO PATIENT CONSEQUENCE REPORTED. THIS REPORT IS FOR A TI TOMOFIX MEDIAL DISTAL FEMUR PLATE-4 HOLES/RIGHT. THIS IS REPORT 2 OF 2 FOR (B)(4).

  Patient problems: No Code Available

  MAUDE report 7669837 ↗