FDA Medical devices recall ·
Philips Allura, Cardio Vascular-Allura Centron recall
- Recall number
- Z-2893-2026
- Date
- (initiated June 17, 2026)
- Company / brand
- Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 257 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
Why was it recalled?
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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(
Distribution
US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2893-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.