Azurion R3.0 Systems
Brand(s)
Last updated
Summary
Product
Azurion R3.0 Systems
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Azurion 7 M20 | Not applicable. | 722234 |
| Azurion 5 M12 | Not applicable. | 722231 |
| Azurion 7 M12 | Not applicable. | 722233 |
| Azurion 3 M12 | Not applicable. | 722229 |
| Azurion 3 M15 | Not applicable. | 722230 |
| Azurion 7 B12 | Not applicable. | 722235 |
| Azurion 7 B20 | Not applicable. | 722236 |
| Azurion 5 M20 | Not applicable. | 722232 |
Issue
Philips has identified nine software issues affecting Azurion R3.0 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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands, 5684 PC
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81381
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