Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT
- Recalling company
- Philips Healthcare (Suzhou) Co., Ltd.
- Product
- Philips Incisive CT
- Reason
- Potential for incomplete scan due to unstable connection inside of floating sensor.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Dec 3, 2025
- Reported
- Jan 14, 2026
- Distribution
- U.S. and U.S. territories
- Status
- Ongoing
- Quantity
- 35
- Company location
- Suzhou
- Recall type
- FDA Mandated
- Recall number
- Z-1003-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1003-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.