GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
FDA Device Recall #Z-1297-2025 — Class II — February 18, 2025
Recall Summary
| Recall Number | Z-1297-2025 |
| Classification | Class II — Moderate risk |
| Date Initiated | February 18, 2025 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | GE Medical Systems, LLC |
| Location | Waukesha, WI |
| Product Type | Devices |
| Quantity | 56 units |
Product Description
GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
Reason for Recall
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
Distribution Pattern
Worldwide distribution.
Lot / Code Information
System ID Number: 907729APEX1, UDI (01)00195278460271(11)231100(21)REV2X2300082CN, Mfg. Lot/Serial Number REV2X2300082CN; System ID Number: 650493REV1, UDI To be provided, Mfg. Lot/Serial Number REVVX1900035CN; System ID Number: 630266CTRV, UDI (01)00195278460271(11)240800(21)REV2X2400093CN, Mfg. Lot/Serial Number REV2X2400093CN; System ID Number: 773702REVCT6ED, UDI (01)00195278460271(11)231000(21)REV2X2300071CN, Mfg. Lot/Serial Number REV2X2300071CN; System ID Number: 312996CTRV2, UDI (01)00195278460271(11)241000(21)REV2X2400126CN, Mfg. Lot/Serial Number REV2X2400126CN; System ID Number: 1000000018, UDI To be provided, Mfg. Lot/Serial Number REV2X2300074CN; System ID Number: 617726Y6REV2, UDI (01)00840682118552(11)170900(21)REVVX1700090CN, Mfg. Lot/Serial Number REVVX1700090CN; System ID Number: 617726Y6REV1, UDI (01)00840682118552(11)160700(21)REVVX1600018CN, Mfg. Lot/Serial Number REVVX1600018CN; System ID Number: 336890APEX, UDI (01)00195278460271(11)240900(21)REV2X2400116CN, Mfg. Lot/Serial Number REV2X2400116CN; System ID Number: 704801APEX, UDI (01)00195278460271(11)241000(21)REV2X2400139CN, Mfg. Lot/Serial Number REV2X2400139CN; System ID Number: 336832APEX, UDI (01)00195278460271(11)241000(21)REV2X2400129CN, Mfg. Lot/Serial Number REV2X2400129CN; System ID Number: 980993CT1, UDI (01)00840682146616(11)210700(21)REV2A2100029CN, Mfg. Lot/Serial Number REV2A2100029CN; System ID Number: 910715REV1, UDI (01)00195278460271(11)241200(21)REV2X2400155CN, Mfg. Lot/Serial Number REV2X2400155CN; System ID Number: 603650APEX1, UDI (01)00195278460271(11)240600(21)REV2X2400068CN, Mfg. Lot/Serial Number REV2X2400068CN; System ID Number: 603526APEX, UDI (01)00195278469700(11)230100(21)REV242200004CN, Mfg. Lot/Serial Number REV242200004CN; System ID Number: 973971REV161, UDI (01)00195278460271(11)241200(21)REV2X2400158CN, Mfg. Lot/Serial Number REV2X2400158CN; System ID Number: 914787APEX, UDI (01)00195278460271(11)231000(21)REV2X2300081CN, Mfg. Lot/Serial Number REV2X2300081CN; System ID Number: 718963EDCT, UDI (01)00195278460271(11)240600(21)REV2X2400070CN, Mfg. Lot/Serial Number REV2X2400070CN; System ID Number: 315473APEX1, UDI (01)00195278460271(11)241100(21)REV2X2400152CN, Mfg. Lot/Serial Number REV2X2400152CN; System ID Number: 614RMHAPEX1, UDI (01)00195278460271(11)240300(21)REV2X2400026CN, Mfg. Lot/Serial Number REV2X2400026CN; System ID Number: 724357APEX, UDI (01)00195278460271(11)230800(21)REV2X2300046CN, Mfg. Lot/Serial Number REV2X2300046CN; System ID Number: 843797REVCT2, UDI (01)00840682123471(11)211100(21)REVV82100041CN, Mfg. Lot/Serial Number REVV82100041CN; System ID Number: 806775APEX, UDI (01)00195278460271(11)231000(21)REV2X2300075CN, Mfg. Lot/Serial Number REV2X2300075CN; System ID Number: 703776APEX, UDI To be provided, Mfg. Lot/Serial Number REV2X2400167CN; System ID Number: 414805REVCT, UDI Not Applicable, Mfg. Lot/Serial Number 00000441066CN8; System ID Number: 262577REVCT, UDI (01)00195278460271(11)240500(21)REV2X2400055CN, Mfg. Lot/Serial Number REV2X2400055CN; System ID Number: 832CT000059, UDI (01)00840682146616(11)220100(21)REV2A2200006CN, Mfg. Lot/Serial Number REV2A2200006CN; System ID Number: 833CT000155, UDI (01)00195278460271(11)240500(21)REV2X2400053CN, Mfg. Lot/Serial Number REV2X2400053CN; System ID Number: AH7084CT02, UDI (01)00840682146616(11)220100(21)REV2A2200007CN, Mfg. Lot/Serial Number REV2A2200007CN; System ID Number: AH1923CT01, UDI (01)00195278460271(11)240300(21)REV2X2400024CN, Mfg. Lot/Serial Number REV2X2400024CN; System ID Number: BG4549CT04, UDI (01)00195278460271(11)230600(21)REV2X2300026CN, Mfg. Lot/Serial Number REV2X2300026CN; System ID Number: E416249APEXCTE, UDI (01)00195278460271(11)231100(21)REV2X2300087CN, Mfg. Lot/Serial Number REV2X2300087CN; System ID Number: 082421140968, UDI To be provided, Mfg. Lot/Serial Number Not Available; System ID Number: 082421140960, UDI (01)00195278633149(11)240500(21)CBFCG2400006HM, Mfg. Lot/Serial Number CBFCG2400006HM; System ID Number: 082421140959, UDI (01)00195278633149(11)240500(21)CBFCG2400004HM, Mfg. Lot/Serial Number CBFCG2400004HM; System ID Number: DK1044CT12, UDI (01)00840682146616(11)200200(21)REV2A2000001CN, Mfg. Lot/Serial Number REV2A2000001CN; System ID Number: DK1547CT01, UDI (01)00840682123471(11)210100(21)REVV82100002CN, Mfg. Lot/Serial Number REVV82100002CN; System ID Number: DK1051CT04, UDI To be provided, Mfg. Lot/Serial Number 00000442412CN3; System ID Number: CT52261701, UDI To be provided, Mfg. Lot/Serial Number REV2X2300050CN; System ID Number: M40230104, UDI (01)00840682118552(11)160600(21)REVVX1600012CN, Mfg. Lot/Serial Number REVVX1600012CN; System ID Number: REV020, UDI To be provided, Mfg. Lot/Serial Number 00000442334CN9; System ID Number: CT00486, UDI (01)00195278460271(11)231000(21)REV2X2300079CN, Mfg. Lot/Serial Number REV2X2300079CN; System ID Number: KRCT54972221, UDI To be provided, Mfg. Lot/Serial Number Not Available; System ID Number: KRCT54893311, UDI To be provided, Mfg. Lot/Serial Number Not Available; System ID Number: 0850211084, UDI To be provided, Mfg. Lot/Serial Number REV2X2300016CN; System ID Number: NO1068CT04, UDI (01)00840682118552(11)171000(21)REVVX1700106CN, Mfg. Lot/Serial Number REVVX1700106CN; System ID Number: P00652CT01, UDI (01)00195278460271(11)240200(21)REV2X2400017CN, Mfg. Lot/Serial Number REV2X2400017CN; System ID Number: PL1672CT03, UDI (01)00840682146616(11)210600(21)REV2A2100019CN, Mfg. Lot/Serial Number REV2A2100019CN; System ID Number: SA1420CT01, UDI To be provided, Mfg. Lot/Serial Number REV2X2400137CN; System ID Number: SA2973CT01, UDI To be provided, Mfg. Lot/Serial Number REV2X23000030CN; System ID Number: CT53972381, UDI To be provided, Mfg. Lot/Serial Number REV2X2400121CN; System ID Number: A201CT07, UDI (01)00195278460271(11)240200(21)REV2X2400014CN, Mfg. Lot/Serial Number REV2X2400014CN; System ID Number: AC001CT05, UDI (01)00840682118552(11)181000(21)REVVX1800101CN, Mfg. Lot/Serial Number REVVX1800101CN; System ID Number: 541010CT02, UDI (01)00840682118552(11)190900(21)REVVX1900106CN, Mfg. Lot/Serial Number REVVX1900106CN; System ID Number: THCTX24524601, UDI (01)00195278460271(11)241000(21)REV2X2400131CN, Mfg. Lot/Serial Number REV2X2400131CN; System ID Number: AE1025CT03, UDI (01)00840682118552(11)210300(21)REVVX2100010CN, Mfg. Lot/Serial Number REVVX2100010CN.
Other Recalls from GE Medical Systems, LLC
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-2154-2026 | Class II | Revolution Apex, X-ray Computed Tomography, Mod... | Mar 26, 2026 |
| Z-2153-2026 | Class II | Revolution CT ES, X-ray Computed Tomography, Mo... | Mar 26, 2026 |
| Z-2149-2026 | Class II | Revolution Ascend, computed tomography, Model N... | Mar 26, 2026 |
| Z-2151-2026 | Class II | Revolution Apex Elite, X-ray Computed Tomograph... | Mar 26, 2026 |
| Z-2150-2026 | Class II | Revolution CT, x-ray computed tomography, Model... | Mar 26, 2026 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.