FDADecember 12, 2023device

Philips Azurion system, Interventional fluoroscopic x-ray system. System Product Name - Model Numbers Azurion 3M12 -722063, 722221; Azurion 3M15 - 722064, 722222; Azurion 5M12 - 722227; Azurion 5M20 - 722228; Azurion 7B12/12 - 722067, 722225; Azurion 7B20/15 - 722068, 722226; Azurion 7M12 - 72207...

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

The hazard

System may exhibit a loss of imaging functionality and data due to an issue which can cause the system to continuously restart. If the issue occurs during a procedure, there may be a delay and/or abortion of the procedure.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380852750088483809920300884838101890008848380852820088483809921000884838099227008848380992340088483805929000884838064775008848380853500088483809926500884838059207

Recall history

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

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