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Philips allura xper systems

Official notice

4 Jun 2026

MediumHealth Canada

An official Health Canada notice concerns Philips allura xper systems. Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection. Published 2026-06-04.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82161

Official notice

2026-06-04

The hazard

Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection.

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.

Skus

722038, 722029, ALLURA XPER FD10, 001443, 722027, 722058, 0708MD02, 722035, 722026, 722028

Other

RA RA-82161

Model Numbers

722038, 722029, ALLURA XPER FD10, 001443, 722027, 722058, 0708MD02, 722035, 722026, 722028

Recall Numbers

82161

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Affected products

Product 1

Lot or serial number - Not applicable., Model or catalogue number - 722038

Product 2

Lot or serial number - Not applicable., Model or catalogue number - 722029

Product 3

Lot or serial number - Not applicable., Model or catalogue number - ALLURA XPER FD10

Product 4

Lot or serial number - Not applicable., Model or catalogue number - 001443

Product 5

Lot or serial number - Not applicable., Model or catalogue number - 722027

Product 6

Lot or serial number - Not applicable., Model or catalogue number - 722058

Product 7

Lot or serial number - Not applicable., Model or catalogue number - 0708MD02

Product 8

Lot or serial number - Not applicable., Model or catalogue number - 722035

Product 9

Lot or serial number - Not applicable., Model or catalogue number - 722026

Product 10

Lot or serial number - Not applicable., Model or catalogue number - 722028

Risk / hazard

Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection.

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

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

82161

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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