NA 7080 Surgical TableRecalls & reported problems
Steris Corporation · 7080 Table, 110-120V, Velcro, Dual Articulating Head, Feather Weight Leg Section, 2-inch TLT Pads · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995229139), received between Jun 4, 2026 and Jul 30, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Key or Button Unresponsive/not Working” (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
- Key or Button Unresponsive/not Working1
- Mechanical Problem1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 30, 2026Key or Button Unresponsive/not Working
The user facility reported that their 7080 Surgical Table was not responding to commands from the hand control during a patient procedure resulting in a procedure delay. The procedure was completed successfully. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50086672 ↗MalfunctionJul 2, 2026Use of Device Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, USER FACILITY PERSONNEL COMMANDED THEIR 7080 SURGICAL TABLE INTO REVERSE TRENDELENBURG AND THE TABLE'S FOOT SECTION "DROPPED QUICKLY" TO THE FLOOR AS WELL AS THE HEAD SECTION. THE PATIENT WAS TRANSFERRED TO ANOTHER TABLE WHERE THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25694915 ↗MalfunctionJun 4, 2026Mechanical Problem
THE USER FACILITY REPORTED THAT WHILE A PATIENT WAS BEING TRANSFERRED ONTO THEIR 7080 SURGICAL TABLE FOR A PROCEDURE, THE TABLE WOULD NOT RESPOND TO COMMANDS. USER FACILITY PERSONNEL UTILIZED ANOTHER SURGICAL TABLE, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25399703 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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