Philips India Intuis Radiology Device Recall

ANSM has formally recorded a medical device safety action by Philips India Limited concerning the RX Intuis interventional radiology system. The action, bearing ANSM reference number R2530744, was communicated to users via a letter from the manufacturer dated 21 April 2026. The safety action letter is available from ANSM upon request.

Radiology departments and interventional radiology services using Philips India RX Intuis devices should monitor for correspondence from the manufacturer. ANSM advises affected users to direct questions to Philips India Limited as the originating issuer of the safety communication.