STERIS 4095 Surigical Table (REF ST013911013)Recalls & reported problems
Steris Corporation · STERIS 4095 TABLE 120V SS FWLS VELCRO 3" PWS PADS · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00724995195250), received between Mar 11, 2022 and May 21, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Sparking” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Sparking1
- Unintended Movement1
- Unintended System Motion1
- Unstable1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2026Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, WHILE USER FACILITY PERSONNEL WERE RAISING THE STERIS 4095 SURGICAL TABLE, THE BASE OF THE TABLE LIFTED OFF THE GROUND. AT THE TIME OF THE EVENT, THE PATIENT WAS POSITIONED AT THE HEAD END OF THE TABLE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25244233 ↗MalfunctionSep 28, 2023Unstable; Unstable
THE USER FACILITY REPORTED THAT WHILE UTILIZING A THIRD-PARTY BEACH CHAIR ACCESSORY WITH THEIR 4095 SURGICAL TABLE DURING A PATIENT PROCEDURE, THE TABLE BECAME UNSTABLE SUBSEQUENTLY CAUSING THE TABLE TO LIFT OFF THE FLOOR AT ONE END. THE PROCEDURE WAS COMPLETED SUCCESSFULLY, AND NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17835856 ↗MalfunctionOct 18, 2022Sparking; Sparking
THE USER FACILITY REPORTED THE POWER SUPPLY TO THEIR PATIENT WARMING SYSTEM PACK SPARKED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15627748 ↗MalfunctionMar 11, 2022Unintended System Motion; Unintended System Motion
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4095 SURGICAL TABLE DRIFTED DOWNWARD AND TO THE RIGHT WITHOUT BEING COMMANDED TO DO SO RESULTING IN A PROCEDURE DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13738977 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page