STERIS 5095 Surgical TableRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995214074), received between Dec 20, 2023 and Jan 2, 2026 — 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.

• MalfunctionJan 2, 2026Unintended Movement

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 5095 SURGICAL TABLE BEGAN TO SLIDE WITHOUT BEING COMMANDED TO DO SO. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23946515 ↗
• MalfunctionDec 20, 2023Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED VIA MEDWATCH REPORT (MW5154308) THAT DURING A PATIENT PROCEDURE, FACILITY PERSONNEL HEARD A LOUD NOISE, AND THEIR 5095 SURGICAL TABLE LIFTED TO THE LEFT WITHOUT BEING COMMANDED TO DO SO. FACILITY STAFF STABILIZED THE TABLE BY PRESSING IT TO THE GROUND. THE PATIENT WAS TRANSFERRED FROM THE TABLE TO A STRETCHER RESULTING IN A PROCEDURE DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18369637 ↗