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No image published for this recall

Umidificatore ad ultrasuoni Ultrasonic humidifier

Official notice

2 Dec 2022

Last checked

2 Dec 2022

Critical riskEU Safety Gate

An official EU Safety Gate notice concerns Umidificatore ad ultrasuoni Ultrasonic humidifier. The non-antibacterial water tank is not accessible for cleaning and the appliance does not emit a warning sound and light to change the water as required. This could lead to the development of mould that can cause allergic reactions when spread by air. The product does not comply with the requirements of the Low Voltage Directive nor with the European standard EN 60335. Published 2022-12-02.

What to do now

The source does not provide specific consumer instructions. Follow the official EU Safety Gate notice for next steps.

Recall number

A12/01672/22

Official notice

2022-12-02

The hazard

The non-antibacterial water tank is not accessible for cleaning and the appliance does not emit a warning sound and light to change the water as required. This could lead to the development of mould that can cause allergic reactions when spread by air. The product does not comply with the requirements of the Low Voltage Directive nor with the European standard EN 60335.

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.

Upcs

8033224603667

Models

BABY LINE, HI3012E

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Affected products

Product 1

Air humidifier

Product 2

Umidificatore ad ultrasuoni / Ultrasonic humidifier

Risk / hazard

The non-antibacterial water tank is not accessible for cleaning and the appliance does not emit a warning sound and light to change the water as required. This could lead to the development of mould that can cause allergic reactions when spread by air. The product does not comply with the requirements of the Low Voltage Directive nor with the European standard EN 60335.

Where it was sold

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

Location 1

DE · Germany

Location 2

FR · France

Affected area 1

DE · Germany

Affected area 2

FR · France

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Laica.

Source & status

Tier

beta

Category

ELECTRONICS

Classification

Serious risk — Microbiological

App estimate

critical

Recall details

Recall number

A12/01672/22

Classification

Serious risk — Microbiological

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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