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Azurion and allura systems

Official notice

30 Jan 2025

Last checked

30 Jan 2025

Medium riskHealth Canada

An official Health Canada notice concerns Azurion and allura systems. Philips has identified that during manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, possibly resulting in an injury of the finger. The risk is applicable for the operators and service personnel. Recall start date: January 17, 2025 Published 2025-01-30.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76885

Official notice

2025-01-30

The hazard

Philips has identified that during manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, possibly resulting in an injury of the finger. The risk is applicable for the operators and service personnel. Recall start date: January 17, 2025

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

76885

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Affected products

Product 1

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

Product 2

Affected products - Allura Xper FD20 OR Table (Product Of AlluraClarity Family), Lot or serial number - Not applicable., Model or catalog number - 722035

Product 3

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

Product 4

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

Product 5

Affected products - Azurion 7 M20, Lot or serial number - Not applicable., Model or catalog number - 722 224 722 079 722234

Product 6

Affected products - Azurion 3 M12, Lot or serial number - Not applicable., Model or catalog number - 722 063 722 221

Product 7

Affected products - Azurion 3 M15, Lot or serial number - Not applicable., Model or catalog number - 722 064 722 222

Product 8

Affected products - Azurion 7 B12, Lot or serial number - Not applicable., Model or catalog number - 722 067 722235 722 225

Product 9

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

Product 10

Affected products - Azurion 7 M12, Lot or serial number - Not applicable., Model or catalog number - 722233 722 223 722 078

Product 11

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

Product 12

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

Product 13

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

Product 14

Affected products - Azurion 7 B20, Lot or serial number - Not applicable., Model or catalog number - 722 226 722236 722 068

Product 15

Affected products - Azurion 5 M12, Lot or serial number - Not applicable., Model or catalog number - 722 227 722231

Product 16

Affected products - Azurion 5 M20, Lot or serial number - Not applicable., Model or catalog number - 722 228 722232

Risk / hazard

Philips has identified that during manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, possibly resulting in an injury of the finger. The risk is applicable for the operators and service personnel. Recall start date: January 17, 2025

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

Manufacturer

Not provided

Phone

Not provided

Brand: Philips, Azurion And Allura.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

76885

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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