Class II
Medical Device Recall: Philips Incisive CT
Philips Healthcare (Suzhou) Co., Ltd. · December 3, 2025
Reason for Recall
Potential for incomplete scan due to unstable connection inside of floating sensor.
Distribution
U.S. and U.S. territories
Quantity Affected
35
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1003-2026
Status: ongoing
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