STERIS 5095 Surigical Table (REF ST015221000)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995195632), received between Oct 25, 2023 and Oct 9, 2024 — classified as 2 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. 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 9, 2024Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 5095 SURGICAL TABLE WAS NOT LEVELING WHEN COMMANDED TO DO SO USING THE HAND CONTROL. THERE WAS NO REPORT OF INJURY OR PROCEDURE DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20407731 ↗
• MalfunctionOct 25, 2023Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, USER FACILITY PERSONNEL COMMANDED THE 5095 SURGICAL TABLE TO RAISE IN HEIGHT. FOLLOWING THE COMMAND, A LOUD "CRACKING" NOISE WAS HEARD. USER FACILITY PERSONNEL OBSERVED THAT THE TABLE'S COLUMN SHROUD COVERS WERE DAMAGED AND ELECTED TO PROCEED WITH THE PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A MINIMAL DELAY, AND NO INJURIES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18008312 ↗