General Electric Med Systems Advantx 1 LC1 Model 45258230 Angiographic X-ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Advantx 1 LC1 Model 45258230 Angiographic X-ray System
Brand
General Electric Med Systems
Lot Codes / Batch Numbers
All serial numbers
Products Sold
All serial numbers
General Electric Med Systems is recalling Advantx 1 LC1 Model 45258230 Angiographic X-ray System due to Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.
Recommended Action
Per FDA guidance
Field modification instructions were issued on 3/24/04 to GE field engineers who are to correct the devices at hospitals. No letter about the correction was sent to the hospitals.
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