Philips Azurion, Allura Xper and Eleva Systems
Last updated
Summary
Product
Philips Azurion, Allura Xper and Eleva 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 catalog number |
|---|---|---|
| MultiDiagnost Eleva - Image Intensifier - TV Image Detector | Not applicable. | 70832 |
| Allura Xper FD20/15 | Not applicable. | 722058 |
| Allura Xper FD10 | Not applicable. | ALLURA XPER FD10 001443 |
| Allura Xper FD20/20 (Product Of Alluraclarity Family) | Not applicable. | 722038 |
| Allura Xper FD20 Or Table (Product Of Alluraclarity Family) | Not applicable. | 722035 |
| Azurion 7 M20 | Not applicable. | 722 224 722 079 |
| Multidiagnost Eleva - Flat Detector - Image Detector | Not applicable. | 70834 |
| Allura Xper FD10/10 (Product Of Alluraclarity Family) | Not applicable. | 722027 |
| Allura Xper FD20 (Product Of Alluraclarity Family) | Not applicable. | 722028 |
| Allura Xper FD20/10 (Product Of Alluraclarity Family) | Not applicable. | 722029 |
| Azurion 7 B12 | Not applicable. | 722 067 |
| Azurion 7 B20 | Not applicable. | 722 226 722 068 |
| Azurion 7 M12 | Not applicable. | 722 223 722 078 |
Issue
It was reported to Philips that after a procedure was completed, the staff began cleaning and transferring the patient to the patient's trolley. While moving the control screen (cs) monitor, one of the hose cable carriers from the monitor's cable carrier came loose and fell, striking an employee on the head. The injured employee sustained a minor concussion and was placed under observation in the hospital for the entire day before being discharged to rest at home.
Recall start date: August 23, 2024
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
Identification number
RA-76014
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