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Philips allura xper, allura centron and azurion systems

Official notice

19 Jan 2024

Last checked

19 Jan 2024

High riskHealth Canada

An official Health Canada notice concerns Philips allura xper, allura centron and azurion systems. Philips has become aware of issues with three (3) components in certain PCs used with the Philips Allura XPER, Allura Centron and/or Azurion systems that may result in a loss of system functionality. Three (3) components of the PCs may not perform as intended due to manufacturing issues. The PCs within your system may have one (or more) of the impacted components. 1. Dimms (dual in-line memory modules): system may stop functioning and imaging may not be possible. 2. Disk bay: System may stop functioning and imaging may not be possible (eg. Unresponsive, frozen images). 3. Framegrabber card: Flexvision monitor may show no viewports, or one or more viewports may show no image, a distorted image, or a frozen image. Also, switching between viewports on the flexvision monitor may be possible. Recall start date: January 5, 2024 Published 2024-01-19.

What to do now

Contact the manufacturer if you require additional information.

Recall number

74931

Official notice

2024-01-19

The hazard

Philips has become aware of issues with three (3) components in certain PCs used with the Philips Allura XPER, Allura Centron and/or Azurion systems that may result in a loss of system functionality. Three (3) components of the PCs may not perform as intended due to manufacturing issues. The PCs within your system may have one (or more) of the impacted components. 1. Dimms (dual in-line memory modules): system may stop functioning and imaging may not be possible. 2. Disk bay: System may stop functioning and imaging may not be possible (eg. Unresponsive, frozen images). 3. Framegrabber card: Flexvision monitor may show no viewports, or one or more viewports may show no image, a distorted image, or a frozen image. Also, switching between viewports on the flexvision monitor may be possible. Recall start date: January 5, 2024

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

74931

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Affected products

Product 1

Affected products - Azurion 7 M12, Lot or serial number - Not applicable., Model or catalog number - 722 223 722 078

Product 2

Affected products - Allura XPER FD20 Or Table (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722023

Product 3

Affected products - Azurion 7 B20, Lot or serial number - Not applicable., Model or catalog number - 722 068

Product 4

Affected products - Allura XPER FD10 (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722026

Product 5

Affected products - Allura XPER FD20/10 (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722029

Product 6

Affected products - Allura XPER FD20/20 OR Table (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722039

Product 7

Affected products - Allura XPER FD20/15, Lot or serial number - Not applicable., Model or catalog number - 722058

Product 8

Affected products - Allura XPER FD20 (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722028

Product 9

Affected products - Allura XPER FD20/20 (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722038

Product 10

Affected products - Azurion 7 M20, Lot or serial number - Not applicable., Model or catalog number - 722 224 722 079

Product 11

Affected products - Allura XPER FD10, Lot or serial number - Not applicable., Model or catalog number - 001443

Product 12

Affected products - Allura XPER FD10/10 (Product Of Alluraclarity Family), Lot or serial number - Not applicable., Model or catalog number - 722027

Product 13

Affected products - Azurion 7 B12, Lot or serial number - Not applicable., Model or catalog number - 722067

Product 14

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

Product 15

Affected products - Azurion 5 M20, Lot or serial number - Not applicable., Model or catalog number - 722228

Risk / hazard

Philips has become aware of issues with three (3) components in certain PCs used with the Philips Allura XPER, Allura Centron and/or Azurion systems that may result in a loss of system functionality. Three (3) components of the PCs may not perform as intended due to manufacturing issues. The PCs within your system may have one (or more) of the impacted components. 1. Dimms (dual in-line memory modules): system may stop functioning and imaging may not be possible. 2. Disk bay: System may stop functioning and imaging may not be possible (eg. Unresponsive, frozen images). 3. Framegrabber card: Flexvision monitor may show no viewports, or one or more viewports may show no image, a distorted image, or a frozen image. Also, switching between viewports on the flexvision monitor may be possible. Recall start date: January 5, 2024

Where it was sold

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

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Philips.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

74931

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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