Recall MonitorHealth Products
Patient Tables of Philips Allura and Azurion systems
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Patient Tables of Philips Allura and Azurion 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 (Product Of Alluraclarity Family) | Not applicable. | 722028 |
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD20/20 (Product Of Alluraclarity Family) | Not applicable. | 722038 |
| Allura Xper FD10/10 (Product Of Alluraclarity Family) | Not applicable. | 722027 |
| Azurion 7 B12 | Not applicable. | 722 067 |
| Allura Xper FD10 (Prouct Of Alluraclarity Family) | Not applicable. | 722026 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| Azurion 7 M20 | Not applicable. | 722 224 722 079 |
| Azurion 7 B20 | Not applicable. | 722 226 722 068 |
| Allura Xper FD10/10 (Product Of Alluraclarity Family) | Not applicable. | 722029 |
| Azurion 7 M12 | Not applicable. | 722 223 722 078 |
Issue
Philips has identified some situations that may result in the patient falling from the table related to the mattress used on the patient table of the Philips Allura and Azurion systems: mattress slipping from the table incorrect positioning of the neuro mattress on the table incorrect mattress being used on the table Recall start date: January 21, 2025