GE Medical Systems, LLC recalls GE Healthcare Optima XR200amx

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.

GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3) A0659MB

GE Healthcare issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 11/25/2024 via letter issued using traceable means. The notice explained the issue, safety issue, and requested the following actions be taken by the user: "1. Perform a check of your device prior to each patient exam to look for the following behaviors. If any are observed, DO NOT use the device and call GE HealthCare Service Immediately. . Column vertical movement requires increased effort. . Column has change in resistance (i.e. movement is not smooth) during vertical movement. . Column makes abnormal noises during vertical movement. 2. Please ensure all potential users in your facility are made aware of this safety notification and the recommended actions. 3. Please retain this document for your records. 4. Please complete and return the attached acknowledgement form to RECALL.10964@gehealthcare.com" For questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative. On 02/11/2025, the firm send an updated notice with a corrected GTIN for Optima XR200amx.

• FDA enforcement recordOfficial FDA database entry for Z-0811-2025
• FDA 510(k) clearance · K103476The device's official FDA premarket clearance record
• FDA 510(k) clearance · K142383The device's official FDA premarket clearance record
• FDA device classification · IZLOfficial FDA classification for this device type
• CFR regulation · 21 CFR 892.1720The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find GE Medical Systems, LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.