Travel cot Recall – EU Safety Gate

Published by Reclia Safety Desk | July 03, 2026

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

Reclia – Recall Information Database
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 travel cot product identified as the “New Mummy Crib Backpack.” The recall is classified as a “Serious risk” under the General Product Safety Regulation. The primary concerns identified in the recall notice are structural instability, a lack of necessary warnings, and a suffocation hazard associated with a supplied cover. The distributor of the product 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 recall notice identifies the following specific hazards associated with the product:

– Injuries (Structural Instability): The product is not structurally stable. The recall notice states that if a baby was left in the product overnight, their natural movements could cause the product to collapse or fall sideways, potentially resulting in injuries.
– Suffocation: The crib is supplied with a cover which would fully enclose and cover the baby. The recall notice explicitly states this poses a potential suffocation risk.
– Non-Compliance: The product does not comply with the General Product Safety Regulation. Specifically, the recall notice indicates the product has no warnings to indicate that it cannot be used overnight.

4. Consumer Action Required

The recall notice specifies that the measure taken is a withdrawal of the product from the market. The exact instructions for consumers who have already purchased this product are not detailed in the provided source data. Consumers are advised to stop using the product immediately and to contact the distributor or retailer from which the product was purchased for further instructions regarding the withdrawal.

5. Official Remedy

The official remedy, as stated in the recall notice, is the withdrawal of the product from the market. The type of economic operator taking the notified measure is the Distributor. The specific remedy for consumers (e.g., refund, replacement) is not specified in the recall notice. The date of entry into force for the measure is listed as “Unknown.”

6. Contact Information

– Case Number: SR/01793/26
– Reference Link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099348
– Notifying Country: United Kingdom in respect of Northern Ireland
– Company Recall Code: Not specified in the recall notice.
– Distributor Information: Not specified in the recall notice.

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