MTS Orthopedic Trauma Top 5855Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842430105999), received between Sep 21, 2023 and Sep 21, 2023 — classified as 1 injury.

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

• InjurySep 21, 2023Adverse Event Without Identified Device or Use Problem; Device Fell; Adverse Event Without Identified Device or Use Problem; Device Fell

  EMPLOYEE ENGAGED IN OPERATING AND MAINTENANCE ACTIVITIES AT A MEDICAL CENTER AND WENT INTO THE OPERATING ROOM EQUIPMENT STORAGE ROOM TO ORGANIZE THE EQUIPMENT FOR THE PLACEMENT OF ANOTHER TABLE. HE ATTEMPTED TO WALK BETWEEN TWO MIZUHO OSI JACKSON ORTHOPEDIC FRACTURE TABLES (MODEL NUMBER (B)(6)) WHICH WERE USED FOR FRACTURED HIP SURGERY. WHILE REPOSITIONING EQUIPMENT, AN UNHOOKED TRACTION ARC BECAME LOOSE THAT CAUSED A POSITIONING LEG HOLDER PIECE TO FALL. THIS PIECE OF EQUIPMENT, WHICH WEIGHTED 20 LBS, FELL OFF A TABLETOP, HITTING EMPLOYEE'S RIGHT FOOT AND INJURING HIS TOE. THE INJURY RESULTED IN A SERIOUS INFECTION. HE WAS TREATED AT A MEDICAL CENTER, WHERE HE UNDERWENT TREATMENT FOR THE TOE INFECTION AND WAS HOSPITALIZED.

  Patient problems: Bacterial Infection

  MAUDE report 17792041 ↗