Recall MonitorHealth Products
Philips Allura Xper Systems
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Philips Allura Xper Systems
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Allura Xper FD20/20 (Product Of AlluraClarity Family) | Not applicable. | 722038 |
| Allura Xper FD20/10 (Product Of AlluraClarity Family) | Not applicable. | 722029 |
| Allura Xper FD10 | Not applicable. | ALLURA XPER FD10 |
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD10/10 (Product Of AlluraClarity Family) | Not applicable. | 722027 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| MultiDiagnost Eleva- Flat Detector - Image Detector | Not applicable. | 0708MD02 |
| Allura Xper FD20 OR Table (Product Of AlluraClarity Family) | Not applicable. | 722035 |
| Allura Xper FD 10 (Product Of AlluraClarity Family) | Not applicable. | 722026 |
| Allura Xper FD20 (Product Of AlluraClarity Family) | Not applicable. | 722028 |
Issue
Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection.