Azurion and Allura Systems
Summary
Contact the manufacturer if you require additional information.
Affected 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 |
Azurion 3 M12 |
Not applicable. |
722 063 |
Azurion 3 M15 |
Not applicable. |
722 064 |
Azurion 7 B12 |
Not applicable. |
722 067 |
Allura Xper FD10/10 (Product Of AlluraClarity Family) |
Not applicable. |
722027 |
Azurion 7 M12 |
Not applicable. |
722233 |
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 |
Azurion 5 M12 |
Not applicable. |
722 227 |
Azurion 5 M20 |
Not applicable. |
722 228 |
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
Additional information
Details
Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands, 5684 PC
Get notified
Receive notifications for new and updated recalls and alerts by category.