FDADecember 8, 2023device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Loss of connectivity between the FlexArm and the Table due to a software issue related to the date/time format. This connection issue leads to a loss of movement of the arm or table.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

0088483808526800884838099258

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12) — Recall Details · AllClear