Amsco 3085 SP Surgical Table (REF ST010101)Recalls & reported problems
Steris Corporation · The AMSCO 3085 SP Surgical Table IA Compatible Tabletop with 2-inch TLT Pads is a mobile, electrohydraulically operated general surgical table providing flexible articulation of the surgical patient. · Class 1
Data updated Oct 16, 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 00724995155049), received between Jun 1, 2023 and Apr 13, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device Tipped Over” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Tipped Over1
- Key or Button Unresponsive/not Working1
- Sharp Edges1
- Unintended Movement1
Patient problems
- Abrasion2
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 13, 2026Unintended Movement
THE USER FACILITY REPORTED THAT DURING THE TRANSFER OF A PATIENT, THEIR 3085 SURGICAL TABLE "TIPPED SLIGHTLY". THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24865947 ↗MalfunctionNov 15, 2025Device Tipped Over; Device Tipped Over
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 3085 SURGICAL TABLE "TIPPED OVER" RESULTING IN A PROCEDURE POSTPONEMENT. THE PATIENT WAS UNINJURED, BUT EMPLOYEES SUFFERED MINOR INJURIES WHILE STABILIZING THE PATIENT BACK ONTO THE TABLE. IT IS UNKNOWN AT THIS TIME WHETHER MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Abrasion
MAUDE report 23563851 ↗MalfunctionNov 6, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 3085 SURGICAL TABLE WOULD NOT RESPOND TO COMMANDS VIA THE HAND CONTROL. USER FACILITY PERSONNEL ATTEMPTED TO UTILIZE ANOTHER HAND CONTROL HOWEVER; THE TABLE WOULD NOT RESPOND TO COMMANDS. USER FACILITY PERSONNEL ELECTED TO PROCEED WITH THE PROCEDURE WHICH WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23489894 ↗MalfunctionJun 1, 2023Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED THAN AN EMPLOYEE WAS CLEANING THE SHROUD GUARD COLUMN PROTECTOR ON A 3085SP SURGICAL TABLE AND OBTAINED A CUT ON THEIR FINGER. A BAND-AID WAS APPLIED; NO ADDITIONAL MEDICAL TREATMENT WAS SOUGHT.
Patient problems: Abrasion
MAUDE report 17037700 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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