Philips Incisive CT Recalled Over Scan Incompletion Risk
Philips Healthcare recalled 35 Incisive CT scanners on December 3, 2025. The devices may produce incomplete scans due to an unstable connection inside the floating sensor. Healthcare providers must stop using these devices immediately and follow recall instructions.
Quick Facts at a Glance
Recall Date
December 3, 2025
Hazard Level
HIGH
Brand
Philips Healthcare
Category
Health & Personal Care
Sold At
Multiple Retailers
At-Risk Groups
GENERAL
Hazard Information
Potential for incomplete scan due to unstable connection inside of floating sensor.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips Healthcare (Suzhou) Co., Ltd. or your healthcare provider for instructions
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Product Details
The recall affects 35 Philips Incisive CT scanners distributed in the U.S. and U.S. territories. The devices were distributed prior to the recall date of December 3, 2025.
The Hazard
The recall stems from a potential for incomplete scans caused by an unstable connection inside the floating sensor. This may compromise diagnostic accuracy, posing a significant risk to patient care.
Reported Incidents
No specific incidents or injuries have been reported in relation to this recall, indicating a proactive measure by Philips.
What to Do
Patients and healthcare providers should stop using the affected devices immediately. Contact Philips Healthcare (Suzhou) Co., Ltd. for further instructions.
Contact Information
For more information, contact Philips Healthcare at 1-800-XXXX-XXXX or visit their website for recall instructions.
Key Facts
Recall date: December 3, 2025
Classification: Class II
Quantity recalled: 35 units
Distribution: U.S. and territories
Hazard: Incomplete scans due to unstable connection
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