Philips Allura Xper
Last updated
Summary
Product
Philips Allura Xper
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 |
|---|---|---|
| Allura Xper FD20 OR Table (Product Of Alluraclarity Family) | Not applicable. | 722035 |
| Allura Xper FD10/10 (Product Of Alluraclarity Family) | Not applicable. | 722027 |
| Allura Xper FD20/10 (Product Of Alluraclarity Family) | Not applicable. | 722029 |
| Allura Xper FD10 | Not applicable. | 001443 |
| Allura Xper FD20 (Product Of Alluraclarity Family) | Not applicable. | 722028 |
Issue
Philips has identified potential safety issues with delayed LTE kit installations for Allura R7.6-R8.1 systems exceeding 10 years of life. The kit includes a propeller motor clamping bolt and the x-ray tube locking bolt. If one of these bolts breaks, part of the system will not function as expected.
Recall Start Date: November 18, 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-76616
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