Philips North America Llc — Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
Official product recall notices and clearly labeled enforcement reference records.
Reference record — not a live warning · enforcement-reference · official-source
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.
- Provider
- FDA — device enforcement reference
- Source observed
- 8/18/2026, 12:00:00 AM UTC
- Source updated
- 9/29/2026, 12:00:00 AM UTC
- Location
- Cambridge, MA, US
- 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.
- notice
- Periodic enforcement reference; not a real-time safety alert or a reliable recall-lifecycle tracker.
- product
- Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
- distribution
- U.S. and U.S. Territories.
- event number
- 99865
- manufacturer
- Philips North America Llc
- recall number
- Z-3155-2026
- source status
- Open, Classified
- freshness minutes
- 180
Source use policy · openFDA reference data; not a real-time public alert service
Update history (1 recent revisions)
- 10/8/2026, 2:10:41 AM UTC
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