Notice names this product. Philips Healthcare (Suzhou) Co’s Philips Incisive CT with software V4 is named in FDA Class II recall Z-2988-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Potential of failing to trigger clinical scan during Bolus Tracking. Identifying details: Device Identifier: (01)00884838085015, (01)00884838105508.. Units affected: N/A. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Potential of failing to trigger clinical scan during Bolus Tracking.
Company / brand: Philips Healthcare (Suzhou) Co recalls
Affected product: Philips Incisive CT with software V4 recall status
Official ID Z-2988-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.