STERIS 4085 Surgical Table (REF ST013307)Recalls & reported problems
Steris Corporation · The STERIS 4085 Table Battery Line ABS Featherweight Leg Section with TLT Pads accommodates virtually all patients with generous weight and height ranges and provides outstanding access for C-Arm, permitting high quality images crucial to cardiothoracic, Orthopedic and neurosurgical procedures. · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00724995154752), received between Dec 20, 2023 and Dec 20, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 20, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, USER FACILITY PERSONNEL COMMANDED THEIR 4085 SURGICAL TABLE TO SLIDE DOWNWARD WHEN THEY HEARD A "POPPING" SOUND FROM THE POWERLIFT BEACH CHAIR TO THE TABLE. USER FACILITY PERSONNEL REMOVED THE PATIENT FROM THE BEACH CHAIR AND TRANSFERRED THE BEACH CHAIR AND PATIENT TO A DIFFERENT SURGICAL TABLE RESULTING IN A PROCEDURE DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18369685 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
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- ORT200 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls12 reports
- MEERA mobile operating table 720001F2MAQUET GmbH · 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
- 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.