1 result for "Philips India Limited"
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Philips India Intuis Radiology Device Recall
ANSM has recorded a safety action by Philips India Limited involving the RX Intuis interventional radiology device. The action, registered under reference R2530744, has been communicated to affected users via letter dated 21 April 2026. ANSM directs users with questions to contact Philips India Limited directly.
Urgent
Enforcement
Medical Devices
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