STERIS 5095 Surigical Table (REF ST015211000)Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995195625), received between Jun 2, 2022 and Nov 21, 2024 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 21, 2024Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 5095 SURGICAL TABLE WAS COMMANDED TO LOWER IN HEIGHT AND HEARD A "NOISE" FROM THE TABLE'S SHROUD. THE PATIENT WAS TRANSFERRED TO A DIFFERENT TABLE. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20751365 ↗
• MalfunctionNov 1, 2024Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, A SMALL AMOUNT OF SMOKE APPEARED FROM THE BASE OF THEIR 5095 SURGICAL TABLE WHILE POSITIONING A PATIENT AND NOTICED THAT THERE APPEARED TO BE A FLUID LEAK. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20589508 ↗
• MalfunctionDec 22, 2022Unintended Movement; Unintended Movement

  THE USER FACILITY REPORTED THAT THEIR 5095 SURGICAL TABLE WOULD NOT RESPOND TO HAND CONTROL COMMANDS. A PROCEDURE DELAY WAS REPORTED. NO INJURIES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16033576 ↗
• MalfunctionJun 2, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE USER FACILITY REPORTED THAT PRIOR TO THE START OF A PATIENT PROCEDURE, HOSPITAL PERSONNEL WERE UTILIZING THE HAND CONTROL TO THEIR 5095 SURGICAL TABLE TO COMMAND THE TABLE TO SLIDE HOWEVER, THE TABLE'S BACK SECTION BEGAN TO MOVE SIDE TO SIDE. HOSPITAL PERSONNEL WERE ABLE TO PLACE THE TABLE IN THE DESIRED POSITION AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO INJURY OR PROCEDURE DELAY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14577634 ↗