Reported Aug 12, 2026 · Ongoing · Updated Sep 16, 2026
Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 6 · Best
Is this the product you have?
- Philips Allura, Cardio Vascular-Allura Centron
- Model Number722400. Interventional Fluoroscopic X-Ray System
- Lot codes and dates
- Model Number722400
- UDI Number
257 of 257 codes
(01)00884838042315(21)282(01)00884838042315(21)206(01)00884838042315(21)187(01)00884838042315(21)486(01)00884838042315(21)480(01)00884838042315(21)71(01)00884838042315(21)322(01)00884838042315(21)506(01)00884838042315(21)429(01)00884838042315(21)413(01)00884838042315(21)497(01)00884838042315(21)507(01)00884838042315(21)502(01)00884838042315(21)222(01)00884838042315(21)144(01)00884838042315(21)510(01)00884838042315(21)190(01)00884838042315(21)43(01)00884838042315(21)439(01)00884838042315(21)176(01)00884838042315(21)76(01)00884838042315(21)364(01)00884838042315(21)209(01)00884838042315(21)382(01)00884838042315(21)178(01)00884838042315(21)243(01)00884838042315(21)16(01)00884838042315(21)110(01)00884838042315(21)4(01)00884838042315(21)101(01)00884838042315(21)131(01)00884838042315(21)93(01)00884838042315(21)156(01)00884838042315(21)347(01)00884838042315(21)552(01)00884838042315(21)482(01)00884838042315(21)414(01)00884838042315(21)80(01)00884838042315(21)112(01)00884838042315(21)42(01)00884838042315(21)127(01)00884838042315(21)407(01)00884838042315(21)33(01)00884838042315(21)184(01)00884838042315(21)153(01)00884838042315(21)189(01)00884838042315(21)424(01)00884838042315(21)201(01)00884838042315(21)245(01)00884838042315(21)122(01)00884838042315(21)273(01)00884838042315(21)228(01)00884838042315(21)79(01)00884838042315(21)307(01)00884838042315(21)476(01)00884838042315(21)108(01)00884838042315(21)533(01)00884838042315(21)250(01)00884838042315(21)272(01)00884838042315(21)252
- Amount recalled
- 257 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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