Amsco 3085-R Surgical TableRecalls & reported problems
Steris Corporation · The AMSCO 3085 General Surgical Table is a mobile, electrohydraulically operated general surgical table providing flexible articulation of the surgical patient. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00724995155025), received between Mar 31, 2022 and Jun 15, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Complete Loss of Power” (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.
Most reported problems
Device problems
- Complete Loss of Power1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 15, 2023Complete Loss of Power; Complete Loss of Power
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 3085-R SURGICAL TABLE LOST POWER. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17137056 ↗MalfunctionMar 31, 2022Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 3085-R SURGICAL TABLE MADE A LOUD NOISE AND BECAME UNSTABLE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13971357 ↗
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.
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