FDADecember 12, 2025device

Philips Azurion system; Software Version Number: R3.1;

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

The hazard

Philips has identified two (2) software issues affecting device systems that may result in loss of imaging (X-ray) functionality and/or loss of motorized movement, and/or incorrect image content and/or loss of data. Issue 1 - System remains in continuous restart mode after the start-up. Issue 2 - Longitudinal Position Error Applicable only to systems with Poly-G3 frontal stand.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

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Recall history

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

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Philips Azurion system; Software Version Number: R3.1; — Recall Details · AllClear