STERIS 5085 Surgical Table (REF ST014107)Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00724995154905), received between Feb 6, 2023 and May 30, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 30, 2025Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE A PATIENT SLID DOWN THEIR 5085 SURGICAL TABLE WHILE THE TABLE WAS IN THE TRENDELENBURG POSITION. THE PATIENT WAS REPOSITIONED ON THE TABLE AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22117491 ↗
• MalfunctionOct 25, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  THE USER FACILITY REPORTED THAT WITH A PATIENT POSITIONED ON THEIR 5085 SURGICAL TABLE, THE LEG SECTION AND X-RAY TOP DROPPED DOWN CAUSING A PROCEDURAL DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY ON THE SAME TABLE. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18007287 ↗
• MalfunctionMay 25, 2023Unintended Movement; Unintended Movement

  THE USER FACILITY REPORTED VIA MEDWATCH # THAT DURING A PATIENT PROCEDURE THEIR 5085 SURGICAL TABLE UNEXPECTEDLY ROTATED LEFT WITHOUT BEING COMMANDED TO DO SO. THE PATIENT WAS CAUGHT BY USER FACILITY PERSONNEL AND EASED DOWN TO THE FLOOR WITHOUT ANY IMPACT. THE PATIENT WAS TRANSFERRED TO ANOTHER TABLE AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17003663 ↗
• MalfunctionFeb 17, 2023Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT AT THE END OF A PATIENT PROCEDURE WITH THEIR 5085 SURGICAL TABLE IN REVERSE TRENDELENBURG THE TABLE WOULD NOT RETURN TO LEVEL AS COMMANDED ON THE HAND CONTROL. USER FACILITY PERSONNEL MANUALLY TRANSFERRED THE PATIENT TO A STRETCHER. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16397376 ↗
• MalfunctionFeb 6, 2023Unintended Movement; Unintended Movement

  THE USER FACILITY REPORTED THAT FOLLOWING A COMPLETED PATIENT PROCEDURE THEIR 5085 SURGICAL TABLE WOULD NOT RETURN TO LEVEL POSITION, INSTEAD THE TABLE MOVED FURTHER INTO TRENDELENBURG POSITION. THE PATIENT WAS REMOVED FROM THE SURGICAL TABLE ONTO A STRETCHER. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16308711 ↗