Class II

Medical Device Recall: Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · May 16, 2024

Reason for Recall

When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.

Distribution

Domestic: OK International: India, Spain, U.A.E.

States Affected

OK

Quantity Affected

1 unit (OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1897-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Medical Device Recall: Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100. | SafeCheck