Fresh Recalls

Philips Healthcare (Suzhou) Co recalls

Recall found. Philips Healthcare (Suzhou) Co is named in FDA Class II recall Z-2988-2026 covering Philips Incisive CT with software V4. Hazard: Potential of failing to trigger clinical scan during Bolus Tracking. Identifying details: Device Identifier: (01)00884838085015, (01)00884838105508.. Status: Ongoing.

Models with recalls

Philips Incisive CT with software V4 (1)

All Philips Healthcare (Suzhou) Co recalls

FDA Class II · Medical device · September 2, 2026

Philips Incisive CT with software V4 recall — Philips Healthcare (Suzhou) Co., Ltd.

Potential of failing to trigger clinical scan during Bolus Tracking.

Official ID Z-2988-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.