Class II

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

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · December 8, 2023

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

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

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0860-2024

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.