FDAJune 4, 2025device

Azurion 7 M20. Fluoroscopic X-Ray System.

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

The hazard

Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838085268

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. Fluoroscopic X-Ray System. — Recall Details · AllClear