Ge Healthcare Discovery CT 750 HD model numbers: 5232083, 5232083-2, 5232083-3, and 5232083-4. For head, whole body, cardiac and vascular X-ray Computed Tomography applications. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Discovery CT 750 HD model numbers: 5232083, 5232083-2, 5232083-3, and 5232083-4. For head, whole body, cardiac and vascular X-ray Computed Tomography applications.
Brand
Ge Healthcare
Lot Codes / Batch Numbers
Serial numbers for the mentioned model numbers manufactured from November 2008 to November 2009.
Products Sold
Serial numbers for the mentioned model numbers manufactured from November 2008 to November 2009.
Ge Healthcare is recalling Discovery CT 750 HD model numbers: 5232083, 5232083-2, 5232083-3, and 5232083-4. For head, whole bo due to Failure to properly document the CTDI in the Technical Reference or User Manual.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to properly document the CTDI in the Technical Reference or User Manual.
Recommended Action
Per FDA guidance
GE is sending an Important Electronic Product Radiation Warning letter to customers. The letter will describe the defect, identify the affected product details, provide instructions, state the product correction, and the necessary contact information.
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