HIGH

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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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Report Date
January 14, 2026
Recall Status
ACTIVE

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