Medrad Inc Stellant CT Injection System. Powered Injector with Syringe. Angiographic Injector and Syringe. Model numbers S, SX, D, and DX Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stellant CT Injection System. Powered Injector with Syringe. Angiographic Injector and Syringe. Model numbers S, SX, D, and DX
Brand
Medrad Inc
Lot Codes / Batch Numbers
all serial numbers
Products Sold
all serial numbers
Medrad Inc is recalling Stellant CT Injection System. Powered Injector with Syringe. Angiographic Injector and Syringe. Mode due to the heat maintainer, an accessory, may overheat and deform the disposable syringe. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
the heat maintainer, an accessory, may overheat and deform the disposable syringe
Recommended Action
Per FDA guidance
The recalling firm issued an Urgent Medical Device Field Correction notice dated 10/12/05 via certified mail. The notice provided instructions to apply warning labels and disconnect the heat maintainer until a field upgrade kit is available. In case where the heat maintainer is a necessity for specific procedures, the customer is being instructed to observe certain precautions.
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