FDA DeviceClass IINotable
FDA Recall: Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurio
Description
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Hazard
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Remedy
3,341 units
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