STERIS 5085 Surgical Table (REF ST014101)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995154875), received between May 4, 2023 and Oct 31, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 31, 2024Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE USER FACILITY PERSONNEL COMMANDED THE FOOT SECTION OF THEIR 5085 SURGICAL TABLE TO LOWER IN HEIGHT. THE FOOT SECTION MOVED "FAST/QUICK" TO THE LOWEST HEIGHT POSITION WITHOUT BEING COMMANDED TO DO SO. USER FACILITY PERSONNEL ELECTED TO CONTINUE THE PATIENT PROCEDURE WITH THE FOOT SECTION IN THE UNDESIRED POSITION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY, AND NO PROCEDURE DELAY OR INJURY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20577650 ↗
• MalfunctionMay 4, 2023Unintended Movement; Unintended Movement

  THE USER FACILITY REPORTED VIA MEDWATCH REPORT MW5116422 THAT DURING A PATIENT PROCEDURE THE TABLETOP TO THEIR 5085 SURGICAL TABLE BEGAN TO MOVE IN AN UNCONTROLLED MANNER. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY OR PROCEDURE DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16867392 ↗