Travel cot Recall – EU Safety Gate

Published by Reclia Safety Desk | July 07, 2026

Here is the factual recall information record based on the provided EU Safety Gate data.

Recall Information Record
Database: Consumer Safety (EU Safety Gate)
Record ID: SR/01793/26
Date of Entry: Based on source data.

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1. Recall Summary

The notifying country, the United Kingdom in respect of Northern Ireland, has issued a recall for a specific travel cot product. The product, identified as the “New Mummy Crib Backpack,” presents risks of injuries and suffocation to infants. The recall notice states that the product is not structurally stable and lacks necessary warnings. The distributor has initiated a measure to withdraw the product from the market.

2. Affected Products

– Product Category: Childcare articles and children’s equipment
– Product Type: Travel cot
– Product Name: New Mummy Crib Backpack
– Brand: Not specified in the recall notice.
– Model/Type Number: Not specified in the recall notice.
– Batch Number: Not specified in the recall notice.
– Barcode: 1600000253844
– Description: A backpack containing a fold-out crib with multiple compartments.
– Country of Origin: People’s Republic of China
– Notifying Country: United Kingdom in respect of Northern Ireland
– Production Dates: Not specified in the recall notice.

3. Hazard Information

The following hazards are explicitly identified in the recall notice:
– Structural Instability: The product is not structurally stable. The notice indicates that if a baby is left in the product overnight, their natural movements could cause the product to collapse or fall sideways, resulting in injuries.
– Suffocation Risk: The crib is supplied with a cover which would fully enclose and cover the baby, potentially leading to suffocation.
– Non-Compliance: The product does not comply with the General Product Safety Regulation.
– Risk Type as Classified: Injuries, Suffocation.
– Risk Level: Serious risk.

4. Consumer Action Required

The recall notice specifies the following action for consumers:
– The product is being withdrawn from the market by the distributor.
– The notice does not provide specific instructions for consumers who have already purchased the product, such as to stop using it immediately or to return it to the place of purchase. The primary action stated is the withdrawal of the product from the market by the economic operator.

5. Official Remedy

– Type of Economic Operator Taking Measure: Distributor
– Category of Measure: Withdrawal of the product from the market.
– Date of Entry into Force: Unknown (not specified in the recall notice).
– Details on Remedy: The official remedy is the withdrawal of the product from the market. No specific remedy for individual consumers (e.g., refund, replacement) is detailed in the provided source data.

6. Contact Information

– Case Number: SR/01793/26
– Reference Link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099348
– Company Recall Code: Not specified in the recall notice.
– Distributor Contact: Not specified in the recall notice. The distributor is the economic operator taking the measure, but specific contact details are not provided in the source data.

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