General Electric Med Systems LLC Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3, 2259973-4. The system consists of a radiographic table, a overhead tube suspension, high frequency generator and power distribution unit, wall stand, dual focal spot x-ray tube and operator''s console. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3, 2259973-4. The system consists of a radiographic table, a overhead tube suspension, high frequency generator and power distribution unit, wall stand, dual focal spot x-ray tube and operator''s console.
Brand
General Electric Med Systems LLC
Lot Codes / Batch Numbers
all serial numbers
Products Sold
all serial numbers
General Electric Med Systems LLC is recalling Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3, 2259973-4. The syst due to Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.
Recommended Action
Per FDA guidance
An 'Urgent: Radiation Safety Notice' letter was issued to hospitals with affected systems describing potential hazards, the planned modification and recommended action to limit the hazard until the planned modification is installed. A GE field Service Representative will install the modification.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026