Philips Allura Xper and Azurion 7 Systems
Summary
Contact the manufacturer if you require additional information.
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 |
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
Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands, 5684 PC
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