Recall MonitorHealth Products
Azurion R3.0 Systems
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Azurion R3.0 Systems
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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.