Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
Published October 7, 2026 · Recall initiated: August 18, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.
What to do
FDA Mandated
Recall details
- Manufacturer
- Philips North America Llc
- Distributor
- U.S. and U.S. Territories.
- Lot
- UDI: (01)00884838101111
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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Questions about this recall
Was Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333 recalled?
Yes. FDA published recall Z-3155-2026 on October 7, 2026. Reported hazard: The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.
What should I do if I have this product?
FDA Mandated
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