Reported Sep 13, 2023 · Ongoing
Azurion
Philips Medical Systems Nederland B.V.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Medical Systems Nederland B.V. · High Tech Campus 36 · Eindhoven, N/A · N/A
Is this the product you have?
- Azurion
- Lot codes and dates
- Azurion series
- Amount recalled
- 5432 systems in total
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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