FDAMarch 21, 2023device

Philips Azurion System with software versions: R2.2.O, R2.2.1, R2.2.3, R2.2.5 and R2.2.6. Models/Model Number: (1) Azurion 3M12: 722063, 722221; (2) Azurion 3M15: 722064, 722222; (3) Azurion SM12: 722227; (4) Azurion SM20: 722228; (5) Azurion 7B12/12: 722067, 722225; (6) Azurion 7820/15: 722068, ...

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

The hazard

Potential Loss of X-ray-When the full disk capacity is reached, X-Ray functionality will cease to be available there will be a sudden interruption of the procedure

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380852750088483809920300884838085282008848380992100088483809922700884838099234008848380853500088483809926500884838085367008848380992720088483808525100884838099241

Recall history

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

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