PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Medical Device Recall in 2024 - (Recall #: Z-0860-2024)

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:

Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)

Product Classification:

Class II

Date Initiated: December 8, 2023

Date Posted: February 7, 2024

Recall Number: Z-0860-2024

Event ID: 93721

Reason for Recall:

Loss of connectivity between the FlexArm and the Table due to a software issue.

Status: Ongoing

Product Quantity: 28 systems (9 US, 1 Canada, 18 ROW)

Code Information:

(1) System Code: 722079; (1) UDI/DI: 00884838085268; (1) Serial Number: 1086, 1392, 703615, 1079, 743, 703456, 1248; (2) System Code: 722224; (2) UDI/DI: 00884838099258; (2) Serial Number: 1337, 1249, 1925, 1250, 468, 379, 647, 633, 1534, 887, 1349, 280, 969, 197, 1177, 455, 3, 2611, 2716, 606, 2025;

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of CO, FL, IL, MS, NV and TX. The country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated