PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)

Recalled February 7, 2024 · FDA recall Z-0860-2024 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V

Hazard

Loss of connectivity between the FlexArm and the Table due to a software issue. · FDA Class II

Units

28 systems (9 US, 1 Canada, 18 ROW)

Sold at

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

Description

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

Product

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

Manufacturer(s)

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Made in

Netherlands

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →