Travel cot Recall – EU Safety Gate

Published by Reclia Safety Desk | July 17, 2026

Recall Information Record – Reclia Database

1. Recall Summary
The European Union Safety Gate system has published a recall notification concerning a travel cot product. The recall was initiated by a distributor in the United Kingdom in respect of Northern Ireland. The case number assigned to this notification is SR/01793/26. The product is classified under the category of childcare articles and children’s equipment. The notifying country is the United Kingdom in respect of Northern Ireland. The country of origin is the People’s Republic of China. The measure taken is the withdrawal of the product from the market. The date of entry into force of the measure is listed as unknown.

2. Affected Products
The affected product is identified as a “New Mummy Crib Backpack.” The product is described as a backpack containing a fold-out crib with multiple compartments. The brand is not specified in the recall notice. The type or model number is not specified in the recall notice. The batch number is not specified in the recall notice. The barcode associated with the product is 1600000253844. The production dates are not specified in the recall notice. The product is a travel cot.

3. Hazard Information
The recall notice identifies the risk type as “Injuries, Suffocation.” The specific danger described in the notice states that the product is not structurally stable. The notice further states that the product has no warnings to indicate that it cannot be used overnight. According to the notice, if a baby were left in the product overnight, their natural movements could cause the product to collapse or fall sideways, potentially resulting in injuries. Additionally, the notice states that the crib is supplied with a cover which would fully enclose and cover the baby, potentially leading to suffocation. The notice also states that the product does not comply with the General Product Safety Regulation. The risk level is classified as “Serious risk” in the source data.

4. Consumer Action Required
The recall notice specifies that the measure taken is the withdrawal of the product from the market. The notice does not provide specific instructions for consumers regarding actions such as returning the product, discontinuing use, or contacting the distributor. The notice does not include a URL for a recall page. The notice does not include a company recall code. The notice does not specify any instructions for consumers to contact the manufacturer or distributor directly.

5. Official Remedy
The official remedy, as stated in the source data, is the withdrawal of the product from the market. The type of economic operator taking the notified measure is the distributor. The category of the measure is withdrawal of the product from the market. No information is provided in the recall notice regarding a refund, replacement, or repair for consumers who have already purchased the product.

6. Contact Information
The recall notice does not provide a phone number, email address, website, or physical address for the manufacturer, distributor, or any other entity for consumer inquiries. The notifying country is the United Kingdom in respect of Northern Ireland. The country of origin is the People’s Republic of China. The brand is not specified in the recall notice. The company recall code is not specified in the recall notice. The reference URL for the Safety Gate alert is: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099348.

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