Philips Incisive CT (Philips Healthcare (Suzhou) Co., Ltd. Suzhou Industrial Park No.) – potential for incomplete scan due to ... (2025)
Potential for incomplete medical scan due to unstable sensor connection.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips Incisive CT
Brand
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Industrial Park No.
Lot Codes / Batch Numbers
N/A
Products Sold
N/A
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Industrial Park No. is recalling Philips Incisive CT due to Potential for incomplete scan due to unstable connection inside of floating sensor.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for incomplete scan due to unstable connection inside of floating sensor.
Recommended Action
Per FDA guidance
Philips will send a customer notification to the existing users of the affected systems to alert them of the issue and provide the actions that should be taken in order to prevent risks to patients. Philips will contact customers to schedule a time for a Philips Field Service Engineer (FSE) to visit their site and install a hardware solution that will change the method of connection for the rear handle floating sensor. Customers who need additional information or support concerning this issue should be directed to their local Philips representative at 1-800-722-9377 (Philips Customer Care Solutions Center). Philips reference: 2025-PD-CTAMI-109 or FCO72800843.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026