Patient Tables of Philips Allura and Azurion systems
Last updated
Summary
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
Affected 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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
| Philips Medical Systems Nederland B.V. |
| Veenpluis 6, Best, Netherlands, 5684 PC |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76910
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