NA Cmax X-ray Imaging TableRecalls & reported problems
Steris · The Cmax X-Ray Imaging Table has a carbon fiber floating tabletop and can be operated in standalone mode or powered patient transfer. · Class 1
Data updated Oct 13, 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 00724995216825), received between Sep 14, 2022 and Apr 30, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Key or Button Unresponsive/not Working1
Patient problems
- Electric Shock1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 30, 2026Key or Button Unresponsive/not Working
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR CMAX X-RAY SURGICAL TABLE DID NOT RESPOND TO HAND CONTROLS COMMANDS. THE PROCEDURE WAS COMPLETED SUCCESSFULLY ON THE SAME TABLE. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25050264 ↗MalfunctionSep 14, 2022Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
THE USER FACILITY REPORTED THAT DURING CLEANING ACTIVITIES AN EMPLOYEE ATTEMPTED TO CONNECT THE POWER CABLE TO THE CMAX X-RAY SURGICAL TABLE AND THEY EXPERIENCED AN ELECTRICAL SHOCK. NO REPORT OF CONSEQUENCE ON HEALTH OF THE EMPLOYEE. DURING THE EVENT, THE TABLE WAS NOT IN USE AND THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: Electric Shock
MAUDE report 15417009 ↗
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
- 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
- TS 7500 2067886Baxter 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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