Water pump Recall – EU Safety Gate

Published by Reclia Safety Desk | July 21, 2026

Recall Information Record – Reclia Database

1. Recall Summary
The European Commission’s Safety Gate system has published a recall notification concerning a water pump product sold under the brand Avansa. The recall was initiated by the manufacturer and reported by the notifying country, Ireland. The case number assigned to this action is SR/01500/26. The product is classified as an electrical appliance and equipment item. The recall became effective on 11 March 2026.

2. Affected Products
The specific product subject to this recall is the Avansa Circulation Pump, model number AVS 32-6 EA 180. The product is described as a red and black electric water circulating pump. The barcode associated with the product is 5949040800179. The product was sold online, in particular via the website www.atria-europe.com. The batch number and production dates are not specified in the recall notice. The country of origin is listed as Unknown.

3. Hazard Information
The recall notice identifies the risk type as “Electric shock.” The stated danger is that, due to incorrect mains electrical coupling, the product poses a risk of electric shock to the user. The recall notice further states that the product does not comply with the requirements of the Low Voltage Directive nor with the European standards EN 60335-1 and EN 60335-2. The risk level is classified by the notifying authority as “Serious risk.”

4. Consumer Action Required
The recall notice specifies that the measure taken is a recall by offering a replacement product. Consumers who have purchased the affected Avansa Circulation Pump, model AVS 32-6 EA 180, should stop using the product immediately. The recall notice does not provide specific instructions for consumers to return the product to a physical store or to contact a specific customer service number. The action required is to participate in the recall process as initiated by the manufacturer, which involves offering a replacement product. No further consumer action steps, such as disconnection procedures or disposal instructions, are detailed in the source data.

5. Official Remedy
The official remedy, as stated in the recall notice, is a recall by offering a replacement product. The type of economic operator taking the notified measure is the manufacturer. The measure category is “Recall by offering a replacement product.” The date of entry into force for this measure is 11 March 2026. No information regarding a refund, repair, or other financial compensation is provided in the source data. The remedy is limited to the provision of a replacement product.

6. Contact Information
The recall notice does not provide a specific telephone number, email address, or physical address for consumer inquiries. The product was sold online via www.atria-europe.com, but no direct contact details for the manufacturer or the seller are included in the recall notice. The notifying country is Ireland. For general inquiries regarding this recall, consumers may refer to the official Safety Gate alert using the reference link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098859. No other contact information is specified in the source data.

Frequently Asked Questions