Published by Reclia Safety Desk | July 21, 2026
📌 EU Safety Gate Recall Notice
Product: Skin lightening cream
Brand: SHINESHINE SKINCARE
Country: Sweden
Hazards: Chemical Risk, Non-Compliance
What to do: Stop using this product. Follow the recall instructions for refund or replacement.
Case #SR/01376/26 |
View original notice →
Recall Summary
| Product | Skin lightening cream |
| Brand | SHINESHINE SKINCARE |
| Country | Sweden |
| Case Number | SR/01376/26 |
| Hazard | Chemical Risk, Non-Compliance |
| Source | 🇪🇺 EU Safety Gate |
Reclia – Recall Information Database Record
1. Recall Summary
This recall notice, case number SR/01376/26, was issued by the notifying country Sweden and published on the EU Safety Gate system. The recall concerns a cosmetic product identified as a skin lightening cream. The product was subject to import rejection at the border. The risk level associated with this product is classified as “Serious risk.” The measure was ordered against the importer of the product. The date of entry into force of the measure is not specified in the recall notice.
2. Affected Products
– Product type: Skin lightening cream
– Brand: SHINESHINE SKINCARE
– Product name: 5D EXTREME Whitening Face Cream
– Category: Cosmetics
– Type / number of model: Not specified in the recall notice
– Batch number: Not specified in the recall notice
– Barcode: Not specified in the recall notice
– Production dates: Not specified in the recall notice
– Country of origin: Not specified in the recall notice
– Notifying country: Sweden
– Case number: SR/01376/26
– Reference link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098837
3. Hazard Information
The recall notice identifies the risk type as “Chemical.” The specific danger stated in the source data is as follows: The product contains hydroquinone, which is prohibited in this cosmetic product. Hydroquinone may cause an allergic skin reaction and might cause cancer and causes serious eye damage. The product does not comply with the Cosmetic Products Regulation.
4. Consumer Action Required
The recall notice does not provide specific instructions for consumers regarding actions they should take with the product. The measure recorded is “Import rejected at border,” meaning the product was intercepted before entering the market in the notifying country. Consumers who may have obtained this product outside of the official market channel should refer to the official remedy and contact information below. No consumer-level recall action (such as return to store or disposal instructions) is explicitly stated in the source data.
5. Official Remedy
The official measure ordered by the competent authority is: “Import rejected at border.” This measure was ordered against the type of economic operator identified as the “Importer.” The remedy prevents the product from being placed on the market in Sweden. No further remedy for consumers (such as refund, replacement, or recall from end users) is specified in the recall notice.
6. Contact Information
– Notifying country: Sweden
– EU Safety Gate alert reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098837
– Case number: SR/01376/26
– Company recall code: Not specified in the recall notice
– Economic operator subject to measure: Importer (specific name and contact details not provided in the source data)
– Manufacturer or distributor contact: Not specified in the recall notice
Additional Notes
– The product image is available at: https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11006947
– The recall notice does not specify the country of origin of the product.
– The recall notice does not provide a batch number, barcode, or production date range.
– The recall notice does not provide a URL for a company-specific recall page.
– The recall notice does not provide a date of entry into force for the measure.
End of Record
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 Skin lightening cream?
A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/01376/26).
Q: What should I do if I own the recalled Skin lightening cream?
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 Skin lightening cream?
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)
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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.