TemporaryFDAOngoing
Can cause harm that is usually temporary.
Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
Check the device or its packaging for
UDI: (01)00884838101111
- Why
- 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.
- Distributed
- U.S. and U.S. Territories.
- Company
- Philips North America Llc
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-3155-2026 · retrieved 29 September 2026
Read the official notice