Philips Allura Centron X-ray System Recalled for Capacitor Failure
Philips is recalling 87 Allura Centron X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the hazard is a functional failure (loss of image acquisition) with no reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Philips North America, LLC is recalling 87 units of the Cardio Vascular-Allura Centron, system code 722400. The recall is due to a potential failure of a capacitor inside the converter of the Velara X-ray generator. This failure may occur after a large number of surges in a short period of time.
When the capacitor fails, no image acquisition is possible. The affected units were distributed nationwide in the United States and worldwide. The source text notes that the specific serial numbers listed were not distributed in the US, though the distribution pattern indicates nationwide domestic distribution.
Healthcare facilities should contact Philips North America, LLC for further instructions regarding the recall. The source text does not specify a remediation method or a specific date for the recall.
The recalled product
- Product
- Cardio Vascular-Allura Centron, system code 722400
- Manufacturer
- Philips North America, LLC
- Hazard
- Affected units
- 87
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 9 recalled by Philips North America, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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