Philips North America, LLC Recall: Cardio Vascular-Allura Centron, system code 722400
Philips North America, LLC Recall: Cardio Vascular-Allura Centron, system code 722400 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips North America, LLC; Product: Cardio Vascular-Allura Centron, system code 722400; Reason for recall: A capacitor inside the converter of the Vela
| Recalling firm | Philips North America, LLC |
|---|---|
| Product | Cardio Vascular-Allura Centron, system code 722400 |
| Reason for recall | A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide domestic distribution. Foreign distribution worldwide. |
| Recall initiated | 20191230 |
| Recall number | Z-1494-2020 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
Try RecallGuard →