Surgigraphic Surgigraphic 6000 TableRecalls & reported problems
Steris Corporation · The SurgicGraphic 6000 Surgical Table is primarily designed for minimally invasive endovascular, vascular, cardiovascular, pain management, and other procedures requiring intra-operative fluoroscopic C-Arm imaging. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995155247), received between Apr 26, 2023 and Aug 14, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (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
- Mechanical Problem1
- Power 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.
MalfunctionAug 14, 2026Power Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50252596 ↗MalfunctionOct 17, 2023Mechanical Problem; Mechanical Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR SURGIGRAPHIC 6000 IMAGE GUIDED SURGICAL TABLE WOULD NOT MOVE IN RESPONSE TO COMMANDS. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17950943 ↗MalfunctionApr 26, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED VIA MEDWATCH REPORT (B)(4), THAT DURING A PATIENT PROCEDURE THEIR SURGIGRAPHIC 6000 IMAGE GUIDED SURGICAL TABLE WOULD NOT RESPOND TO HAND CONTROL COMMANDS. USER FACILITY PERSONNEL PROCEEDED TO UTILIZE THE SURGICAL TABLE AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16817265 ↗
Other TABLE, OPERATING-ROOM, ELECTRICAL devices
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- TS 7000 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall22 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall9 reports
- Head-Positioning accessories 1739994Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall1 report
- TS 7500 2067886Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall0 reports
- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 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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