STERIS 4085 Surgical Table (REF ST013501)Recalls & reported problems
Steris Corporation · The STERIS 4085 Table Battery Line 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
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995154776), received between Feb 2, 2023 and Nov 3, 2023 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem2
- Device Tipped Over1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 3, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE PATIENT SLID OFF THE 4085 SURGICAL TABLE ONTO THE FLOOR. THE USER FACILITY STATED THAT THE BACK OF THE TABLE "POPPED UP" AS THE PATIENT WAS LOWERED TO THE FLOOR. DETAILS OF INJURY WERE NOT DISCLOSED. THE TABLE WAS REMOVED FROM SERVICE AND THE PROCEDURE WAS CANCELLED.
Patient problems: Insufficient Information
MAUDE report 18066614 ↗MalfunctionJul 6, 2023Device Tipped Over; Device Tipped Over
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, USER FACILITY PERSONNEL DISENGAGED THE FLOOR LOCKS TO THEIR 4085 SURGICAL TABLE CAUSING THE TABLE TO BEGIN TO TIP. THE TABLE WAS STABILIZED, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17267867 ↗MalfunctionJun 21, 2023Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4085 SURGICAL TABLE SLOWLY MOVED INTO TRENDELENBURG POSITION WITHOUT BEING COMMANDED TO DO SO. THE PROCEDURE WAS COMPLETED SUCCESSFULLY, AND THE TABLE WAS REMOVED FROM SERVICE. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17170502 ↗MalfunctionFeb 2, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE WITH THE PATIENT IN REVERSE ORIENTATION THEIR 4085 SURGICAL TABLE "SNAPPED" AND THE PATIENT FELL OFF THE TABLE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16287058 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls21 reports
- 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.