Class II
Medical Device Recall: Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, 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 (US)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1895-2024
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.