FDAJuly 15, 2024device

Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for Image guidance in diagnostic, interventional, and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular, and n...

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

The hazard

Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to Perform Cold Restart

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380852750088483808528200884838085350008848380853670088483808525100884838085268

Recall history

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

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