Immediate withdrawal of the Suavinex Baby Cologne Memories children's cologne: batch 24100513 exceeds the threshold for limonene, linalool, and geraniol

The AEMPS orders the withdrawal of batch 24100513 (100 ml) of Suavinex Baby Cologne Memories due to undeclared substances: limonene, linalool, and geraniol above the legal limit.

05 of may of 2026 at 09:19h
Immediate withdrawal of the Suavinex Baby Cologne Memories children's cologne: batch 24100513 exceeds the threshold for limonene, linalool, and geraniol
Immediate withdrawal of the Suavinex Baby Cologne Memories children's cologne: batch 24100513 exceeds the threshold for limonene, linalool, and geraniol

The Spanish Agency of Medicines and Medical Devices has ordered the immediate withdrawal from the market of a specific batch of children's cologne from the brand Suavinex. The measure affects the product Baby Cologne Memories due to the detection of undeclared substances on its labeling that pose a risk to health.

The affected batch is 24100513 and corresponds to containers with a capacity of 100 milliliters. Health authorities have acted swiftly after confirming the presence of three hidden allergens in the formulation of the cosmetic intended for babies.

Undeclared allergens exceed legal threshold

Laboratory analyses revealed concentrations higher than 0.001% of limonene, linalool, and geraniol. This level exceeds the limit established by the European regulation on cosmetic products which requires informing of their presence in the list of ingredients.

The omission of this data on the packaging generates a real danger for sensitive consumers. The risk is considerably aggravated because the product is specifically designed for the delicate skin of the child population.

"The lack of this information represents a serious risk to the health of sensitive people" - AEMPS

The manufacturer Suavinex Group has already begun the process of recovering the marketed units. The company is working with distributors to remove the affected items from physical and online points of sale.

Return protocol activated for consumers

The health authorities of all autonomous communities have received the official notification to facilitate the application of the corrective measure. This coordination allows for the rapid identification of establishments that could still have stock of the defective product.

Those who have a colony of this batch at home should stop using it immediately. The official recommendation is to return the item to the store where it was purchased or to contact the responsible company directly to arrange for a replacement or refund.

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