The Recall Desk
HighFDA (Devices)·Z-1303-2025·Announced 2025-03-19

GE Healthcare CT Scanner Systems Recalled Due to Coolant Leak Risk

GE Healthcare is recalling 21 Revolution CT and Revolution Apex series CT systems due to potential coolant fluid leaks near the gantry base. The leaking fluid poses a slip-and-fall hazard if not cleaned up promptly.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is a risk-of-harm medical device recall with no reported illnesses or injuries. Per the severity rubric, medical device recalls involving slip-and-fall hazards where injury has not yet been reported are classified as High (Score 3).

Plain-English summary

GE Healthcare is recalling 21 Revolution CT and Revolution Apex series CT systems (model GE Healthcare Revolution CT ES). The affected units can develop coolant fluid (glycol) leaks from the gantry base area.

The leaking coolant fluid is visible as a blue-colored liquid. While the fluid is not corrosive and does not reach harmful temperatures, it creates a slip-and-fall hazard if not promptly noticed and cleaned up. This recall addresses the risk of injury from falls on the wet floor.

These systems have been distributed worldwide. The recall includes 21 specific units with documented serial numbers and unit identifiers provided by the manufacturer.

Facility operators should contact GE Healthcare to arrange inspection and repair of affected units. Until repairs are complete, facility staff should monitor the gantry base area for fluid leaks and promptly clean any spills to prevent falls.

The recalled product

Product
GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed
Manufacturer
GE Medical Systems, LLC
Category
Medical Device — Medical Imaging / CT Scanner
Hazard
  • coolant-leak
  • slip-fall

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • System ID Number 907729APEX1
  • UDI (01)00195278460271(11)231100(21)REV2X2300082CN
  • Mfg. Lot/Serial Number REV2X2300082CN
  • System ID Number 650493REV2
  • UDI To be provided
  • Mfg. Lot/Serial Number REVVX1900036CN
  • System ID Number 864512APEX1
  • UDI (01)00195278460271(11)240500(21)REV2X2400059CN
  • Mfg. Lot/Serial Number REV2X2400059CN
  • System ID Number 832325REV
  • UDI (01)00195278460271(11)241000(21)REV2X2400134CN
  • Mfg. Lot/Serial Number REV2X2400134CN
  • System ID Number 281MWREVCT
  • Mfg. Lot/Serial Number REVVX1900008CN
  • System ID Number 713792ACT39
  • Mfg. Lot/Serial Number REVV82100006CN
  • System ID Number 206320REV
  • Mfg. Lot/Serial Number 00000441459CN5
  • System ID Number 206320REV2
  • Mfg. Lot/Serial Number REVV82200025CN

Distribution

Distribution scope not specified by the agency.

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