Hair dye Recall – EU Safety Gate

Published by Reclia Safety Desk | July 07, 2026

Recall Information Record – Reclia Database Entry

Case Number: SR/01646/26
Date of Entry: Based on EU Safety Gate alert reference 10098982
Notifying Country: Austria

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1. Recall Summary

The notifying country of Austria has issued a recall for a cosmetic product identified as “Henna Permanent Powder Hair Colour” under the brand name ProfixOrganics. The recall was initiated by the retailer due to the product’s non-compliance with the Cosmetic Products Regulation. The product poses a chemical risk to consumers. The recall applies to end users, meaning consumers who have purchased this product are advised to stop using it immediately. The date of entry into force of the measure is listed as unknown in the official recall notice.

2. Affected Products

– Product Name: Henna Permanent Powder Hair Colour
– Brand: ProfixOrganics
– Product Type: Hair dye (permanent henna powder)
– Description: Permanent henna powder hair dye colour black, 60g.
– Batch Number: 098292
– Barcode: 4053743392488
– Type/Model Number: Not specified in the recall notice.
– Country of Origin: India
– Production Dates: Not specified in the recall notice.
– Company Recall Code: Not specified in the recall notice.

3. Hazard Information

The product has been identified as presenting a chemical risk. According to the official EU Safety Gate data, the product contains p-phenylenediamine without coupler components. This substance is described in the recall notice as potentially genotoxic and a skin sensitizer when in prolonged contact on the hair in contact with the scalp. Additionally, the product contains “brilliant green,” which is also identified as a skin sensitizer and is not authorised for use in hair dye under the Cosmetic Products Regulation. The product does not comply with the Cosmetic Products Regulation.

4. Consumer Action Required

Consumers who have purchased the affected product should take the following action as specified in the recall notice: The measure taken is a recall of the product from end users. Consumers should stop using the product and follow the instructions provided by the retailer or the notifying authority. Specific instructions for returning the product or disposing of it are not detailed in the recall notice beyond the recall measure itself.

5. Official Remedy

The official remedy, as stated in the recall notice, is a recall of the product from end users. The type of economic operator taking the notified measure is the retailer. The category of measure is a recall of the product from end users. Details regarding whether the remedy includes a refund, replacement, or other compensation are not specified in the recall notice.

6. Contact Information

– Notifying Country: Austria
– EU Safety Gate Alert Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098982
– Case Number: SR/01646/26
– Retailer Contact Information: Not specified in the recall notice.
– Manufacturer Contact Information: Not specified in the recall notice.
– Consumer Hotline or Website: Not specified in the recall notice.

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Disclaimer: This record is compiled exclusively from the official EU Safety Gate data provided. No independent testing, verification, or editorial analysis has been performed by Reclia. For the most current information, consumers should refer to the official EU Safety Gate alert or contact the notifying authority in Austria.

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