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Updated 2026-10-07

Philips North America Llc recalls Philips Medical Systems Technologies Ltd. Spectral CT 7500,

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Recalled Product

Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333

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Hazard / Issue

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.

Issued by

FDA

Distribution: U.S. and U.S. Territories.
Lot/Code Info: UDI: (01)00884838101111

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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