Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT
- Recall date
- December 3, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1003-2026
- FDA classification
- Class II
- Brand / firm
- Philips Healthcare (Suzhou) Co., Ltd.
- Sold / distributed
- U.S. and U.S. territories
Why it was recalled
Potential for incomplete scan due to unstable connection inside of floating sensor.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips Incisive CT
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