WhichRecall
Class IIReported 2026-01-14

Philips Incisive CT

Recalled by Philips Healthcare (Suzhou) Co., Ltd.

Reason for Recall

Potential for incomplete scan due to unstable connection inside of floating sensor.

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Recall Number
Z-1003-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-12-03
Reported
2026-01-14
Distribution
U.S. and U.S. territories
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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