Patient Tables of Philips Allura and Azurion systems
Summary
Contact the manufacturer if you require additional information.
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 |
Azurion 7 B20 |
Not applicable. |
722 226 |
Allura Xper FD10/10 (Product Of Alluraclarity Family) |
Not applicable. |
722029 |
Azurion 7 M12 |
Not applicable. |
722 223 |
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
Philips Medical Systems Nederland B.V. |
Veenpluis 6, Best, Netherlands, 5684 PC |
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