Public recall detail

Azurion Systems

2026-05-07

medium
Radiology Performance
Quick summary

Quick summary: Azurion Systems. Reason: Performance. Category: Radiology. Date: 2026-05-07.

Recommended action

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

Recall details

Quick summary: Azurion Systems. Reason: Performance. Category: Radiology. Date: 2026-05-07.

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.
ProductAzurion Systems
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82045

Affected products

ProductAzurion 7 M12
LotNot applicable.
Model722 078
Serial numberNot applicable.
DescriptionAzurion 7 M12
ProductAzurion 7 B12
LotNot applicable.
Model722 067
Serial numberNot applicable.
DescriptionAzurion 7 B12
ProductAzurion 7 M20
LotNot applicable.
Model722 224
Serial numberNot applicable.
DescriptionAzurion 7 M20
ProductAzurion 7 M20
LotNot applicable.
Model722 079
Serial numberNot applicable.
DescriptionAzurion 7 M20

Issue

Philips has identified that the float tabletop control on the control module of Azurion systems may experience mechanical wear over time. The float tabletop control is located on the control module at the table-side. When the control is actuated, the table brakes disengage, allowing adjustment of the longitudinal or transverse position of the table. Over time, mechanical wear may lead to detachment, cracking, or breakage of the float tabletop control, which may lead to reduced availability or unavailability of longitudinal and transverse tabletop movement, as well as the formation of sharp edges.

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 date2026-04-30
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82045
Background{}
CompaniesPhilips Medical Systems Nederland B.V. Veenpluis 6, Best, Netherlands, 5684 PC
AudiencesHealthcare
Source updated2026-05-07

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

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