FDA-Device2019-08-07Class II
Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
Philips Medical Systems Nederlands
Hazard
Philips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR 1003.2(b)(1). When performing Cine runs, the Azurion's automatic exposure control software may set technique factors that result in radiation emissions too low to obtain useful diagnostic images.
Sold states
Nationwide
Affected count
229
Manufactured in
Veenpluis 4-6, N/A, Best, N/A, Netherlands
Products
Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1997-2019Don't want to check this manually?
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