Philips Allura recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)

Medical deviceClass IIOngoing

Summary: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is recalling Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.. Reason: Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

What is being recalled

Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

Why

Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution.

How to tell if yours is affected

Model Number: 722400. 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What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

More recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · all medical device recalls · recalls from June 2026

Official FDA record