STERIS 5095 Surigical Table (REF ST015210002)Recalls & reported problems
Steris Corporation · The STERIS 5095 General Surgical Table SS with Velcro 2-inch TLT Pads is a flexible design gives OR staff the versatility they need to perform a wide range of surgeries using a variety of patient positions. · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995195694), received between Feb 22, 2025 and Sep 17, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Unintended Movement1
Patient problems
- Bruise/Contusion1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Unintended Movement
The user facility reported that during a patient procedure their 5095 Surgical Table ¿rolled away¿. No report of injury or procedure delay.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50802787 ↗MalfunctionFeb 22, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A BRUISE AFTER THE HEAD SECTION FELL FROM THEIR 5095 SURGICAL TABLE AND LANDED ON THE EMPLOYEE'S FOOT. MEDICAL TREATMENT WAS ADMINISTERED WITH AN ICE PACK AND THE EMPLOYEE RETURNED TO WORK.
Patient problems: Bruise/Contusion
MAUDE report 21440983 ↗
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- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.