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No image published for this recall

Philips allura xper and azurion 7 systems

Official notice

13 Jul 2023

Last checked

13 Jul 2023

Medium riskHealth Canada

An official Health Canada notice concerns Philips allura xper and azurion 7 systems. Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: • Loss of bluetooth connection due to interferences from other radio equipment • Battery not fully charged • Battery not holding its charge • Damage in the charger, cable and/or connector of the wireless foot switch Recall start date: July 4, 2023 Published 2023-07-13.

What to do now

Contact the manufacturer if you require additional information.

Recall number

73951

Official notice

2023-07-13

The hazard

Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: • Loss of bluetooth connection due to interferences from other radio equipment • Battery not fully charged • Battery not holding its charge • Damage in the charger, cable and/or connector of the wireless foot switch Recall start date: July 4, 2023

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

73951

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Affected products

Product 1

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

Product 2

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

Product 3

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

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 FD20/15, Lot or serial number - Not applicable., Model or catalog number - 722058

Product 6

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

Product 7

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

Product 8

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

Risk / hazard

Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: • Loss of bluetooth connection due to interferences from other radio equipment • Battery not fully charged • Battery not holding its charge • Damage in the charger, cable and/or connector of the wireless foot switch Recall start date: July 4, 2023

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

73951

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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