Philips Allura Xper Imaging Systems Recalled for Short-Circuit Risk

What You Should Do

1. This recall affects Philips Allura Xper medical imaging systems including models FD10, FD10C, FD10F, FD10/10, FD20, FD20 Biplane, FD20 OR Table, FD20/10, and FD20/20.
2. Identify if your system is affected by checking the model number and serial number on the identification label located on the device. See the Affected Products section below for the full list of affected codes.
3. Stop using the recalled device. Contact Philips or your local distributor to arrange for a technician to inspect the system and install the necessary drip tray if it is missing.
4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this safety alert.

Your Remedy Options

Affected Products