PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Medical Device Recall in 2024 - (Recall #: Z-1897-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 16, 2024

Date Posted: June 5, 2024

Recall Number: Z-1897-2024

Event ID: 94647

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.

Status: Ongoing

Product Quantity: 1 unit (OUS)

Code Information:

Product number: 722013, UDI/DI: 00884838059061; Serial Number: 232.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated