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Updated 2026-09-02

Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0, Product Code 72

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Recalled Product

Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.

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Hazard / Issue

Potential of failing to trigger clinical scan during Bolus Tracking.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Device Identifier: (01)00884838085015, (01)00884838105508.

✅ 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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