Class II

Medical Device Recall: Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.

Philips Healthcare (Suzhou) Co., Ltd. · June 26, 2026

Reason for Recall

Potential of failing to trigger clinical scan during Bolus Tracking.

Distribution

U.S. Nationwide and U.S. Territories distribution.

States Affected

NATIONWIDE

Quantity Affected

N/A

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2988-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Philips Healthcare (Suzhou) Co., Ltd. Medical Device Recall: Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144. | SafeCheck