Philips Allura recall
Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
Why was Philips Allura recalled?
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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, 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(01)00884838042315(21)230, (01)00884838042315(21)548, (01)00884838042315(21)523, (01)00884838042315(21)299, (01)00884838042315(21)494, (01)00884838042315(21)286, (01)00884838042315(21)488, (01)00884838042315(21)541, (01)00884838042315(21)543, (01)00884838042315(21)427, (01)00884838042315(21)447, (01)00884838042315(21)344, (01)00884838042315(21)542, (01)00884838042315(21)262, (01)00884838042315(21)536, (01)00884838042315(21)469, (01)00884838042315(21)529, (01)00884838042315(21)554, (01)00884838042315(21)555, (01)00884838042315(21)546, (01)00884838042315(21)375, (01)00884838042315(21)534, (01)00884838042315(21)433, (01)00884838042315(21)463, (01)00884838042315(21)443, (01)00884838042315(21)483, (01)00884838042315(21)357, (01)00884838042315(21)374, (01)00884838042315(21)277, (01)00884838042315(21)530, (01)00884838042315(21)337, (01)00884838042315(21)549, (01)00884838042315(21)441, (01)00884838042315(21)320, (01)00884838042315(21)445, (01)00884838042315(21)287, (01)00884838042315(21)556, 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(01)00884838042315(21)538, (01)00884838042315(21)197, (01)00884838042315(21)19, (01)00884838042315(21)36, (01)00884838042315(21)415, (01)00884838042315(21)300, (01)00884838042315(21)8, (01)00884838042315(21)3, (01)00884838042315(21)151, (01)00884838042315(21)227, (01)00884838042315(21)528, (01)00884838042315(21)259, (01)00884838042315(21)152, (01)00884838042315(21)330, (01)00884838042315(21)264, (01)00884838042315(21)193, (01)00884838042315(21)44, (01)00884838042315(21)462, (01)00884838042315(21)551, (01)00884838042315(21)396, (01)00884838042315(21)460, (01)00884838042315(21)522, (01)00884838042315(21)249, (01)00884838042315(21)244, (01)00884838042315(21)478, (01)00884838042315(21)499, (01)00884838042315(21)515, (01)00884838042315(21)271, (01)00884838042315(21)306, (01)00884838042315(21)435, (01)00884838042315(21)501, (01)00884838042315(21)518, (01)00884838042315(21)140, (01)00884838042315(21)226, (01)00884838042315(21)360, (01)00884838042315(21)370.
- Product
- Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Quantity
- 257 units
- Distribution
- US Nationwide distribution.
- Recall date
- August 12, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)