Philips Healthcare (Suzhou) Co., Ltd.: Device Recall
Recall #Z-1003-2026 · 12/03/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1003-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Philips Healthcare (Suzhou) Co., Ltd.
- Status
- Ongoing
- Date Initiated
- 12/03/2025
- Location
- Suzhou, China
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 35
Reason for Recall
Potential for incomplete scan due to unstable connection inside of floating sensor.
Product Description
Philips Incisive CT
Distribution Pattern
U.S. and U.S. territories
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.