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Azurion r2.1.10 and r2.2.10 systems

Official notice

29 Dec 2025

Last checked

29 Dec 2025

Critical riskHealth Canada
Watch Philips

An official Health Canada notice concerns Azurion r2.1.10 and r2.2.10 systems. Philips has identified six software issues affecting Azurion R2.1.10 and R2.2.10 systems that may result in loss of imaging (x-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data. Issue 1 - System keeps restarting when the patient database in the Azurion system's suite PC, which stores metadata about patients, studies, procedures, and series objects, contains more than 50,000 series objects, system functionality becomes unavailable. The Azurion system then initiates a recovery restart, but because the number of series objects remains unchanged, the issue persists and the system repeatedly performs recovery restarts. No message is displayed to indicate this situation. Issue 2 - AMC triple drive Due to a firmware issue in the advanced motion controller (AMC) 3-axis drive: movements of the stand might be slow - when this occurs the message "adjustment of frontal stand is required" is displayed to the user, and 3D scan functionality is not available. The message "rotational scanning is unavailable. Reselect the x-ray protocol" is displayed to the user. Motorized movements of the stand might become unavailable - when this occurs, the message "adjustment of frontal stand is required" is shown to the user. Issue 3 - C-partition of suite PC running out of free space The C-drive of the Azurion suite PC may gradually lose available space due to the accumulation of printer spool files. The windows operating system creates a spool file for each print job and deletes it after successful completion. If a print job fails, the spool files are not removed and accumulate after each system (re)start as Windows retries the job, consuming disk space. When the system (re)starts and the C-drive is full, motorized movements are disabled. The following messages appear on the screen "some geometry movements are not available" and "the geometry is starting. Do not change sid". Issue 4 - System remains in continuous restart mode after the start-up Due to a software issue, the license manager (LM) - which verifies installed licenses and enables optional functionality in the Azurion system based on the available licenses - expands the Windows registry database at every system start or restart. Over time, the registry may grow beyond the maximum size that the LM can load. When this happens, the LM cannot start and the system will enter a continuous reboot loop. The Azurion system will not complete booting, and the message "x-ray system is booting..." remains displayed on the screen. Issue 5 - Misalignment of marker tool overlay - applicable only to Azurion systems with the marker tool option When geometry movement exceeds predefined thresholds (e.g., angulation or rotation differences greater than 10°, or a beam-isocenter-to-patient deviation greater than 50 mm), markers are hidden. When the geometry returns within the threshold, markers reappear. However, they may not be restored to their exact original position and can deviate by several millimeters. If the marker tool is used during a clinical procedure to indicate the correct placement of a device, this deviation could lead to incorrect placement of the device. Issue 6 - Longitudinal position error - applicable only to Azurion systems with poly-g3 frontal stand when requesting a movement of the frontal stand in longitudinal direction, the Azurion system may detect a mismatch between the expected longitudinal (set-) position and the measured (actual) position of the stand. This mismatch is caused by a glitch in the longitudinal position value provided by the position sensing potentiometer. When the mismatch is detected, the motion power to the frontal stand is automatically cut off. The message "some stand movements are not available" is displayed to the user. Published 2025-12-29.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81433

Official notice

2025-12-29

The hazard

Philips has identified six software issues affecting Azurion R2.1.10 and R2.2.10 systems that may result in loss of imaging (x-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data. Issue 1 - System keeps restarting when the patient database in the Azurion system's suite PC, which stores metadata about patients, studies, procedures, and series objects, contains more than 50,000 series objects, system functionality becomes unavailable. The Azurion system then initiates a recovery restart, but because the number of series objects remains unchanged, the issue persists and the system repeatedly performs recovery restarts. No message is displayed to indicate this situation. Issue 2 - AMC triple drive Due to a firmware issue in the advanced motion controller (AMC) 3-axis drive: movements of the stand might be slow - when this occurs the message "adjustment of frontal stand is required" is displayed to the user, and 3D scan functionality is not available. The message "rotational scanning is unavailable. Reselect the x-ray protocol" is displayed to the user. Motorized movements of the stand might become unavailable - when this occurs, the message "adjustment of frontal stand is required" is shown to the user. Issue 3 - C-partition of suite PC running out of free space The C-drive of the Azurion suite PC may gradually lose available space due to the accumulation of printer spool files. The windows operating system creates a spool file for each print job and deletes it after successful completion. If a print job fails, the spool files are not removed and accumulate after each system (re)start as Windows retries the job, consuming disk space. When the system (re)starts and the C-drive is full, motorized movements are disabled. The following messages appear on the screen "some geometry movements are not available" and "the geometry is starting. Do not change sid". Issue 4 - System remains in continuous restart mode after the start-up Due to a software issue, the license manager (LM) - which verifies installed licenses and enables optional functionality in the Azurion system based on the available licenses - expands the Windows registry database at every system start or restart. Over time, the registry may grow beyond the maximum size that the LM can load. When this happens, the LM cannot start and the system will enter a continuous reboot loop. The Azurion system will not complete booting, and the message "x-ray system is booting..." remains displayed on the screen. Issue 5 - Misalignment of marker tool overlay - applicable only to Azurion systems with the marker tool option When geometry movement exceeds predefined thresholds (e.g., angulation or rotation differences greater than 10°, or a beam-isocenter-to-patient deviation greater than 50 mm), markers are hidden. When the geometry returns within the threshold, markers reappear. However, they may not be restored to their exact original position and can deviate by several millimeters. If the marker tool is used during a clinical procedure to indicate the correct placement of a device, this deviation could lead to incorrect placement of the device. Issue 6 - Longitudinal position error - applicable only to Azurion systems with poly-g3 frontal stand when requesting a movement of the frontal stand in longitudinal direction, the Azurion system may detect a mismatch between the expected longitudinal (set-) position and the measured (actual) position of the stand. This mismatch is caused by a glitch in the longitudinal position value provided by the position sensing potentiometer. When the mismatch is detected, the motion power to the frontal stand is automatically cut off. The message "some stand movements are not available" is displayed to the user.

How to check if you're affected

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Lots

128, 151, 188, Not applicable, 265, 275, 459, 485, 149, 296, 704

Skus

722 223, 722 078, 722 224, 722 079, 722 067, 722 227, 722 063, 722 221, 722 068, 722 226, 722 228, 722 064, 722 222

Other

RA RA-81433

Model Numbers

722 223, 722 078, 722 224, 722 079, 722 067, 722 227, 722 063, 722 221, 722 068, 722 226, 722 228, 722 064, 722 222

Recall Numbers

81433

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Affected products

Product 1

Affected products - Azurion 7 M12, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 223

Product 2

Affected products - Azurion 7 M12, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 078

Product 3

Affected products - Azurion 7 M20, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 224

Product 4

Affected products - Azurion 7 M20, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 079

Product 5

Affected products - Azurion 7 B12, Lot or serial number - 128, Model or catalogue number - 722 067

Product 6

Affected products - Azurion 7 B12, Lot or serial number - 151, Model or catalogue number - 722 067

Product 7

Affected products - Azurion 7 B12, Lot or serial number - 188, Model or catalogue number - 722 067

Product 8

Affected products - Azurion 5 M12, Lot or serial number - Not applicable, Model or catalogue number - 722 227

Product 9

Affected products - Azurion 3 M12, Lot or serial number - Not applicable, Model or catalogue number - 722 063

Product 10

Affected products - Azurion 3 M12, Lot or serial number - Not applicable, Model or catalogue number - 722 221

Product 11

Affected products - Azurion 7 B20, Lot or serial number - 265, Model or catalogue number - 722 068

Product 12

Affected products - Azurion 7 B20, Lot or serial number - 275, Model or catalogue number - 722 068

Product 13

Affected products - Azurion 7 B20, Lot or serial number - 459, Model or catalogue number - 722 068

Product 14

Affected products - Azurion 7 B20, Lot or serial number - 485, Model or catalogue number - 722 068

Product 15

Affected products - Azurion 7 B20, Lot or serial number - 149, Model or catalogue number - 722 226

Product 16

Affected products - Azurion 7 B20, Lot or serial number - 296, Model or catalogue number - 722 226

Product 17

Affected products - Azurion 7 B20, Lot or serial number - 704, Model or catalogue number - 722 226

Product 18

Affected products - Azurion 5 M20, Lot or serial number - Not applicable., Model or catalogue number - 722 228

Product 19

Affected products - Azurion 3 M15, Lot or serial number - Not applicable., Model or catalogue number - 722 064

Product 20

Affected products - Azurion 3 M15, Lot or serial number - Not applicable., Model or catalogue number - 722 222

Product 21

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 223

Product 22

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 078

Product 23

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 224

Product 24

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 722 079

Product 25

Lot or serial number - 128, Model or catalogue number - 722 067

Product 26

Lot or serial number - 151, Model or catalogue number - 722 067

Product 27

Lot or serial number - 188, Model or catalogue number - 722 067

Product 28

Lot or serial number - Not applicable, Model or catalogue number - 722 227

Product 29

Lot or serial number - Not applicable, Model or catalogue number - 722 063

Product 30

Lot or serial number - Not applicable, Model or catalogue number - 722 221

Product 31

Lot or serial number - 265, Model or catalogue number - 722 068

Product 32

Lot or serial number - 275, Model or catalogue number - 722 068

Product 33

Lot or serial number - 459, Model or catalogue number - 722 068

Product 34

Lot or serial number - 485, Model or catalogue number - 722 068

Product 35

Lot or serial number - 149, Model or catalogue number - 722 226

Product 36

Lot or serial number - 296, Model or catalogue number - 722 226

Product 37

Lot or serial number - 704, Model or catalogue number - 722 226

Product 38

Lot or serial number - Not applicable., Model or catalogue number - 722 228

Product 39

Lot or serial number - Not applicable., Model or catalogue number - 722 064

Product 40

Lot or serial number - Not applicable., Model or catalogue number - 722 222

Risk / hazard

Philips has identified six software issues affecting Azurion R2.1.10 and R2.2.10 systems that may result in loss of imaging (x-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data. Issue 1 - System keeps restarting when the patient database in the Azurion system's suite PC, which stores metadata about patients, studies, procedures, and series objects, contains more than 50,000 series objects, system functionality becomes unavailable. The Azurion system then initiates a recovery restart, but because the number of series objects remains unchanged, the issue persists and the system repeatedly performs recovery restarts. No message is displayed to indicate this situation. Issue 2 - AMC triple drive Due to a firmware issue in the advanced motion controller (AMC) 3-axis drive: movements of the stand might be slow - when this occurs the message "adjustment of frontal stand is required" is displayed to the user, and 3D scan functionality is not available. The message "rotational scanning is unavailable. Reselect the x-ray protocol" is displayed to the user. Motorized movements of the stand might become unavailable - when this occurs, the message "adjustment of frontal stand is required" is shown to the user. Issue 3 - C-partition of suite PC running out of free space The C-drive of the Azurion suite PC may gradually lose available space due to the accumulation of printer spool files. The windows operating system creates a spool file for each print job and deletes it after successful completion. If a print job fails, the spool files are not removed and accumulate after each system (re)start as Windows retries the job, consuming disk space. When the system (re)starts and the C-drive is full, motorized movements are disabled. The following messages appear on the screen "some geometry movements are not available" and "the geometry is starting. Do not change sid". Issue 4 - System remains in continuous restart mode after the start-up Due to a software issue, the license manager (LM) - which verifies installed licenses and enables optional functionality in the Azurion system based on the available licenses - expands the Windows registry database at every system start or restart. Over time, the registry may grow beyond the maximum size that the LM can load. When this happens, the LM cannot start and the system will enter a continuous reboot loop. The Azurion system will not complete booting, and the message "x-ray system is booting..." remains displayed on the screen. Issue 5 - Misalignment of marker tool overlay - applicable only to Azurion systems with the marker tool option When geometry movement exceeds predefined thresholds (e.g., angulation or rotation differences greater than 10°, or a beam-isocenter-to-patient deviation greater than 50 mm), markers are hidden. When the geometry returns within the threshold, markers reappear. However, they may not be restored to their exact original position and can deviate by several millimeters. If the marker tool is used during a clinical procedure to indicate the correct placement of a device, this deviation could lead to incorrect placement of the device. Issue 6 - Longitudinal position error - applicable only to Azurion systems with poly-g3 frontal stand when requesting a movement of the frontal stand in longitudinal direction, the Azurion system may detect a mismatch between the expected longitudinal (set-) position and the measured (actual) position of the stand. This mismatch is caused by a glitch in the longitudinal position value provided by the position sensing potentiometer. When the mismatch is detected, the motion power to the frontal stand is automatically cut off. The message "some stand movements are not available" is displayed to the user.

Where it was sold

The source does not list specific retailers. See the official notice for where affected vehicles were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Philips

Manufacturer

Not provided

Phone

Not provided

Brand: Philips.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

critical

Recall details

Recall number

81433

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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