Philips North America Llc recalls Philips Medical Systems Technologies Ltd. Spectral CT 7500
- Recalling company
- Philips North America Llc
- Product
- Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 18, 2026
- Reported
- Oct 7, 2026
- Distribution
- U.S. and U.S. Territories.
- Status
- Ongoing
- Quantity
- 62
- Lot / codes
- UDI: (01)00884838101111
- Company location
- Cambridge, MA
- Recall type
- FDA Mandated
- Recall number
- Z-3155-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3155-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.