Philips Radiology Device Safety Alert
Summary
The French ANSM has been informed of a safety action initiated by Philips Medical Systems Nederland BV concerning radiology devices. Affected users have received a direct communication from the company regarding this action, registered under ANSM reference R2606927.
What changed
The French National Agency for Medicines and Health Products Safety (ANSM) has issued a safety alert regarding a specific action undertaken by Philips Medical Systems Nederland BV concerning their radiology interventionnel devices, including the RX Azurion, Allura Xper, Allura Centron, and Allura CV20 models. This alert, registered under reference R2606927, indicates that Philips has directly communicated with the affected users. The ANSM is providing this information to imaging and interventional radiology services.
Healthcare providers utilizing these Philips radiology devices should review the communication from Philips Medical Systems Nederland BV, which was provided on March 20, 2026. For any specific questions or concerns related to this safety action, direct contact with Philips Medical Systems Nederland BV is advised. The ANSM's role here is informational, highlighting the company-initiated safety measure.
What to do next
- Review Philips Medical Systems Nederland BV safety communication dated March 20, 2026.
- Contact Philips Medical Systems Nederland BV directly for any questions regarding the safety action.
Archived snapshot
Mar 20, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Information n° R2606927 destinée aux services d’imagerie et radiologie interventionnelle L'ANSM a été informée de la mise en œuvre d’une action de sécurité effectuée par la société Philips Medical Systems Nederland BV.
Les utilisateurs concernés ont reçu le courrier ci-joint.
Cette action de sécurité est enregistrée à l’ANSM sous le n° R2606927. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société Philips Medical Systems Nederland BV (20/03/2026)
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