PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura
- Recalling company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Product
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 17, 2026
- Reported
- Aug 12, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 257 units
- Lot / codes
- Model Number: 722400. UDI Number: (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(
- Company location
- Best
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2893-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2893-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.