Philips Allura under the following System Descriptions and corresponding model numbers recall

Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura Xper FD10C; Model Number: 722001. 5. Allura Xper FD20; Model Numbers: 722006, 722012, 722028. 6. Allura Xper FD20 Biplane; Model Numbers: 722008, 722013. 7. Allura Xper FD20 Biplane OR Table; Model Number: 722025. 8. Allura Xper FD20 OR Table; Model Numbers: 722015, 722023, 722035. 9. Allura Xper FD20/10; Model Number: 72202…

Quantity: 5,012 units

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Company

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best

Date

Wednesday, August 12

Severity

Class II
the product could cause temporary or reversible health problems.

Where sold

Nationwide
US Nationwide distribution.

Status

Ongoing

Recall number

Z-2891-2026

Source

U.S. Food and Drug Administration