Public recall detail

Allura Xper FD10

2026-07-08

medium
Health products Health product recall
Quick summary

Quick summary: Allura Xper FD10. Reason: Health product recall. Category: Health products. Date: 2026-07-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Allura Xper FD10. Reason: Health product recall. Category: Health products. Date: 2026-07-08.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ProductAllura Xper FD10
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82292

Affected products

ProductAllura Xper FD10
LotNot applicable.
Model001443
Serial numberNot applicable.
DescriptionAllura Xper FD10

Issue

Philips has identified through customer complaints that, during certain repair or service actions, Hard Disk Drives (HDD) with different performance characteristics than those specified by the legal manufacturer may have been installed. These HDDs may exhibit reduced reliability over time, which may result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement or loss of data. In addition, Philips has identified that in some Allura systems, HDDs compliant with specifications but of different types have been used within a single system, whereas specifications require identical HDD types. While these systems are not in line with the released configuration, Philips confirms that this does not result in any noticeable performance impact or safety risk.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesPhilips Medical Systems Nederland B.V.Veenpluis 6, Best, Netherlands, 5684 PC
Recall date2026-06-25
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82292
Background{}
CompaniesPhilips Medical Systems Nederland B.V.Veenpluis 6, Best, Netherlands, 5684 PC
AudiencesHealthcare
Source updated2026-07-08

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

Starting...

Related recalls

Similar recalls and safety notices.

Loading related recalls...