FDAJanuary 2, 2024device

Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064 722222; Azurion 5 M20 722228; A...

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

The hazard

Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

0088483808527500884838086777008848380992030088483808528200884838099210008848380992340088483805929000884838064775008848380853500088483809926528293741537200884838059207

Recall history

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

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Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064 722222; Azurion 5 M20 722228; A... — Recall Details · AllClear