Deodorant Recall – EU Safety Gate

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Published by Reclia Safety Desk | July 14, 2026

📌 EU Safety Gate Recall Notice

Product: Deodorant

Brand: FA

Country: Czechia

Hazards: Chemical Risk, Strangulation Hazard, Non-Compliance

What to do: Stop using this product. Follow the recall instructions for refund or replacement.

🇪🇺 Official EU Safety Gate Recall Notice
Case #SR/01458/26 |
View original notice →

Recall Summary

Product Deodorant
Brand FA
Country Czechia
Case Number SR/01458/26
Hazard Chemical Risk, Strangulation Hazard, Non-Compliance
Source 🇪🇺 EU Safety Gate

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

Reclia Recall Information Record
Case Number: SR/01458/26
Date of Record: Based on measure entry into force 22/04/2026

1. Recall Summary
This recall concerns a cosmetic product, specifically an antiperspirant deodorant, marketed under the brand FA. The product is named “ISLAND VIBES” and is identified by the batch number 0925995238 and barcode 9000101092202. The recall was initiated in Czechia following a notification to the EU Safety Gate system. The product originates from Germany. The official measure ordered for this product is destruction.

2. Affected Products
– Product Type: Antiperspirant deodorant (150 ml)
– Brand: FA
– Product Name: ISLAND VIBES
– Type/Model Number: BALI kiss, MANGO – VANILLA BLOSSOM SCENT
– Batch Number: 0925995238
– Barcode (EAN): 9000101092202
– Notifying Country: Czechia
– Country of Origin: Germany
– Production Dates: Not specified in the recall notice.
– Company Recall Code: Not specified in the recall notice.

3. Hazard Information
The recall notice identifies a chemical risk associated with this product. According to the list of ingredients, the product contains the substance 2-(4-tert-butylbenzyl) propionaldehyde (BMHCA). The source data explicitly states that BMHCA is prohibited in cosmetic products under the Cosmetic Products Regulation. The specific hazards attributed to BMHCA in the recall notice are:
– It may harm the reproductive system.
– It may harm the health of the unborn child.
– It may cause skin sensitisation.
The product does not comply with the Cosmetic Products Regulation.

4. Consumer Action Required
The recall notice specifies that the measure ordered for this product is destruction. The type of economic operator to whom the measure was ordered is a retailer. The source data does not provide specific instructions for consumers regarding returning the product or contacting the manufacturer. Consumers who possess this product should verify if it matches the batch number and barcode listed in the Affected Products section. Based on the official measure, consumers should not use the product.

5. Official Remedy
The official remedy ordered by the relevant authority is the destruction of the product. The measure was ordered against a retailer. The date of entry into force for this measure is 22/04/2026. No information regarding a refund, replacement, or other consumer compensation is specified in the recall notice.

6. Contact Information
– EU Safety Gate Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098940
– Notifying Country: Czechia
– Case Number: SR/01458/26
– Brand: FA
– Specific consumer contact details (phone, email, website) for the manufacturer or distributor: Not specified in the recall notice.

Recall Timeline

  • **Current** – Recall announced via EU Safety Gate
  • **Ongoing** – Consumers advised to stop using product
  • **Ongoing** – Refund or replacement available from manufacturer

Frequently Asked Questions

Q: How do I identify the recalled Deodorant?

A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/01458/26).

Q: What should I do if I own the recalled Deodorant?

A: The recall notice advises consumers to stop using the product immediately and follow the recall instructions.

Q: How do I get a refund or replacement for the recalled Deodorant?

A: Contact the manufacturer or retailer using the information in the recall notice.

Q: What are the health risks from this chemical hazard?

A: The recall notice identifies specific chemicals of concern. Contact a healthcare provider if you have health concerns.

Related EU Recalls (Click to expand)

Disclaimer: Information on this page is summarized from official EU Safety Gate recall notices.
Reclia is a recall information database and does not conduct product testing, safety certification,
or independent investigations.

Consumers should refer to the original EU Safety Gate notice
for complete details and official instructions.




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