Health product recall

Allura Systems

Last updated

Summary

Product
Allura 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
Allura Xper FD10 (Product Of Alluraclarity Family) All lots. 722026
Allura Xper FD20/20 OR Table (Product Of Alluraclarity Family) All lots. 722039
Allura Xper FD10/10 (Product Of Alluraclarity Family) All lots. 722027
Allura Xper FD20/15 OR Table All lots. 722 059
Allura Xper FD20 (Product Of Alluraclarity Family) All lots. 722028
Allura Xper FD20/10 (Product Of Alluraclarity Family) All lots. 722029
Allura Xper FD20/20 (Product Of Alluraclarity Family) All lots. 722038
Allura Xper FD20/15 All lots. 722058
Allura Xper FD10 OR Table (Product Of Alluraclarity Family) All lots. 722033
Allura Xper FD20 OR Table (Product Of Alluraclarity Family) All lots. 722035

Issue

Philips has identified a software issue in the internal communication process between the system software and the x-ray generator firmware which may lead to temporary loss of imaging (x-ray) functionality. This issue may be triggered under either of the following situations: 

Situation 1 - Pedal tap: When the foot switch is pressed and released rapidly without generating x-rays (due to a short duration of contact), the system may enter a state where x-ray generation is inhibited. When this occurs, the system does not show any message to the user indicating that x-ray is not possible. A warm restart may resolve the situation in some cases. A cold restart will always resolve the situation. This issue can lead to a delay in therapy.

Situation 2 - Phase fault: Allura systems are designed to automatically recover from phase faults (a phase fault is an abnormal condition in which one or more phase voltages drop to (near) zero). When a phase fault occurs, the x-ray generator software initiates an automatic recovery process to restore fully system functionality, during which imaging (x-ray) functionality is not available for approximately 5 seconds. When the identified software issue occurs during this recovery, communication with the system software is lost, resulting in the system not recognizing that the generator has recovered and is ready for operation. In this situation, the system shows the user message "generator is busy starting up, no x-ray possible". If the phase fault is detected by the generator during acquisition, the system also shows the message "run aborted: tube problem". to restore system functionality a cold restart of the system is required.

These issues affect the Allura Xper systems with software release 8.2 or higher, equipped with a Certeray generator.

Recall start date: July 7, 2025

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-77749

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