Philips Allura Xper Systems
Last updated
Summary
Product
Philips Allura Xper 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 |
|---|---|---|
| Allura Xper FD20/20 (Product Of AlluraClarity Family) | Not applicable. | 722038 |
| Allura Xper FD20/10 (Product Of AlluraClarity Family) | Not applicable. | 722029 |
| Allura Xper FD10 | Not applicable. | ALLURA XPER FD10 |
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD10/10 (Product Of AlluraClarity Family) | Not applicable. | 722027 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| MultiDiagnost Eleva- Flat Detector - Image Detector | Not applicable. | 0708MD02 |
| Allura Xper FD20 OR Table (Product Of AlluraClarity Family) | Not applicable. | 722035 |
| Allura Xper FD 10 (Product Of AlluraClarity Family) | Not applicable. | 722026 |
| Allura Xper FD20 (Product Of AlluraClarity Family) | Not applicable. | 722028 |
Issue
Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection.
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-82161
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