Philips Azurion and Allura Systems
Last updated
Summary
Product
Philips Azurion and Allura 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 catalog numbe |
|---|---|---|
| Model or catalog numbe | Not applicable. | 722 224 722 079 |
| Allura Xper FD10 (Product Of AlluraClarity Family) | Not applicable. | 722026 |
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD20 Or Table (Part Of AlluraClarity Family) | Not applicable. | 722035 |
| Allura Xper FD20 (Product Of AlluraClarity Family) | Not applicable. | 722028 |
Issue
Due to the forces applied during the movement of the C-arc of the Azurion and Allura systems, the bolts supporting the flexmove carriage may become loose and/or break, and cracks may appear in the flexmove carriage.
Recall start date : June 12, 2023
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-73869
Get notified
Receive notifications for new and updated recalls and alerts by category.