TemporaryFDAOngoing
Can cause harm that is usually temporary.
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Check the device or its packaging for
Device Identifier: (01)00884838085015, (01)00884838105508.
- Why
- Potential of failing to trigger clinical scan during Bolus Tracking.
- Distributed
- U.S. Nationwide and U.S. Territories distribution.
- Company
- Philips Healthcare (Suzhou) Co., Ltd.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2988-2026 · retrieved 21 August 2026
Read the official notice