Recall MonitorHealth Products
Azurion and Allura Systems
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Azurion and Allura 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 catalog number |
|---|---|---|
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD20 OR Table (Product Of AlluraClarity Family) | Not applicable. | 722035 |
| Allura Xper FD20/10 (Product Of AlluraClarity Family) | Not applicable. | 722029 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| Azurion 7 M20 | Not applicable. | 722 224 722 079 722234 |
| Azurion 3 M12 | Not applicable. | 722 063 722 221 |
| Azurion 3 M15 | Not applicable. | 722 064 722 222 |
| Azurion 7 B12 | Not applicable. | 722 067 722235 722 225 |
| Allura Xper FD10/10 (Product Of AlluraClarity Family) | Not applicable. | 722027 |
| Azurion 7 M12 | Not applicable. | 722233 722 223 722 078 |
| Allura Xper FD10 (Product Of AlluraClarity Family) | Not applicable. | 722026 |
| Allura Xper FD20 (Product Of AlluraClarity Family) | Not applicable. | 722028 |
| Allura Xper FD20/20 (Product Of AlluraClarity Family) | Not applicable. | 722038 |
| Azurion 7 B20 | Not applicable. | 722 226 722236 722 068 |
| Azurion 5 M12 | Not applicable. | 722 227 722231 |
| Azurion 5 M20 | Not applicable. | 722 228 722232 |
Issue
Philips has identified that during manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, possibly resulting in an injury of the finger. The risk is applicable for the operators and service personnel. Recall start date: January 17, 2025