Philips Allura Xper and Azurion 7 Systems
Last updated
Summary
Product
Philips Allura Xper and Azurion 7 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 number |
|---|---|---|
| Allura Xper FD20 Or Table (Product Of Alluraclarity Family) | Not applicable. | 722035 |
| Allura Xper FD10 (Product Of Alluraclarity Family) | Not applicable. | 722026 |
| Azurion 7 M20 | Not applicable. | 722 224 722 079 |
| Allura Xper FD20/20 (Product Of Alluraclarity Family) | Not applicable. | 722038 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| Allura Xper FD20 (Product Of Alluraclarity Family) | Not applicable. | 722028 |
| Azurion 7 M12 | Not applicable. | 722 078 |
| Allura Xper FD10 | Not applicable. | 001443 |
Issue
Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are:
• Loss of bluetooth connection due to interferences from other radio equipment
• Battery not fully charged
• Battery not holding its charge
• Damage in the charger, cable and/or connector of the wireless foot switch
Recall start date: July 4, 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-73951
Get notified
Receive notifications for new and updated recalls and alerts by category.