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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1
Recalled June 5, 2024 · FDA recall Z-1897-2024 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V
Hazard
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. · FDA Class II
Units
1 unit (OUS)
Sold at
Domestic: OK International: India, Spain, U.A.E.
Description
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.
Product
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.
Manufacturer(s)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →