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Philips azurion, allura xper and eleva systems

Official notice

9 Sept 2024

Last checked

9 Sept 2024

Medium riskHealth Canada

An official Health Canada notice concerns Philips azurion, allura xper and eleva systems. It was reported to Philips that after a procedure was completed, the staff began cleaning and transferring the patient to the patient's trolley. While moving the control screen (cs) monitor, one of the hose cable carriers from the monitor's cable carrier came loose and fell, striking an employee on the head. The injured employee sustained a minor concussion and was placed under observation in the hospital for the entire day before being discharged to rest at home. Recall start date: August 23, 2024 Published 2024-09-09.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76014

Official notice

2024-09-09

The hazard

It was reported to Philips that after a procedure was completed, the staff began cleaning and transferring the patient to the patient's trolley. While moving the control screen (cs) monitor, one of the hose cable carriers from the monitor's cable carrier came loose and fell, striking an employee on the head. The injured employee sustained a minor concussion and was placed under observation in the hospital for the entire day before being discharged to rest at home. Recall start date: August 23, 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

76014

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Affected products

Product 1

Affected products - MultiDiagnost Eleva - Image Intensifier - TV Image Detector, Lot or serial number - Not applicable., Model or catalog number - 70832

Product 2

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

Product 3

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

Product 4

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

Product 5

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

Product 6

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

Product 7

Affected products - Multidiagnost Eleva - Flat Detector - Image Detector, Lot or serial number - Not applicable., Model or catalog number - 70834

Product 8

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

Product 9

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

Product 10

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

Product 11

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

Product 12

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

Product 13

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

Risk / hazard

It was reported to Philips that after a procedure was completed, the staff began cleaning and transferring the patient to the patient's trolley. While moving the control screen (cs) monitor, one of the hose cable carriers from the monitor's cable carrier came loose and fell, striking an employee on the head. The injured employee sustained a minor concussion and was placed under observation in the hospital for the entire day before being discharged to rest at home. Recall start date: August 23, 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 II

App estimate

medium

Recall details

Recall number

76014

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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