Health Canada16 Jul 2026
Philips Allura Xper FD series
Health Canada published a recall notice for Philips Allura Xper FD series on 16 Jul 2026. It is one of 311 notices of this kind from Health Canada since 2 Apr 2026 in AreaZine's record.
Recall
The recall notice
- Issued by
- Health Canada
- Issued
- 16 Jul 2026
- Recall type
- Health product recall
- Companies
- Philips Medical Systems Nederland B.V.Veenpluis 6, Best, Netherlands, 5684 PC
- Official source
- Health Canada: the notice at its source
The latest from Health CanadaEvery warning and recall in Canada
Source: Health Canada: the notice at its source. AreaZine rebuilds this page from the agency's record; the agency's page is the one to act on. Contains information licensed under the Open Government Licence – Canada.
The notice as issued
Issue: Philips has identified a potential safety issue affecting Allura R8.2 systems equipped with a AD7x patient table type potentially leading to loss of geometry movements. In some cases, following a system (re)start, manual and motorized geometry movements may be disabled due to a firmware issue in the Advanced Motion Controller (AMC) single-axis motion control unit used in the AD7x tables of Allura R8.2 systems. When the issue occurs, no message is displayed to the user. In this situation, X-ray imaging is available. The issue can be resolved by performing a cold restart of the system or by restarting the geometry. Additional information Details Original published date: 2026-07-16 Affected products: Affected products Lot or serial number Model or catalogue number Allura Xper FD20 (Product Of Alluraclarity Family) Not applicable. 722028 Allura Xper FD20/20 (Product Of Alluraclarity Family) Not applicable. 722038 Allura Xper FD20/15 Not applicable. 722058 Allura Xper FD10 (Product Of Alluraclarity Family) Not applicable. 722026 Issue
Source: Health Canada: the notice at its source. The text is the agency's, unedited. Contains information licensed under the Open Government Licence – Canada.