Cushion Recall – EU Safety Gate

Published by Reclia Safety Desk | July 17, 2026

📌 EU Safety Gate Recall Notice

Product: Cushion

Brand: House Doctor

Country: Sweden

Hazards: Chemical Risk, 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/01524/26 |
View original notice →

Recall Summary

Product Cushion
Brand House Doctor
Country Sweden
Case Number SR/01524/26
Hazard Chemical Risk, Non-Compliance
Source 🇪🇺 EU Safety Gate

Recall Information Record – EU Safety Gate Database

Case Number: SR/01524/26
Date of Entry: Based on measures effective from 25/06/2025 and 12/08/2025
Notifying Country: Sweden
Database Reference: Reclia – Consumer Safety Information

1. Recall Summary

The product “Society of Lifestyle Cushion w. filling,” brand House Doctor, has been voluntarily withdrawn from the market by the distributor and the importer in Sweden. The recall was initiated due to the presence of perfluorocarboxylic acid related compounds (PFCAs) in the product. The product does not comply with the REACH Regulation. The recall notice was issued by the Swedish notifying authority and is recorded in the EU Safety Gate system.

2. Affected Products

Product: Cushion with filling
Brand: House Doctor
Name: Society of Lifestyle Cushion w. filling
Type/Model Number: 262360060
Barcode: 5707644785182
Batch Number: Not specified in the recall notice.
Production Dates: Not specified in the recall notice.
Country of Origin: People’s Republic of China
Description: Army green cushion with filling. The product was sold online, in particular via www.royaldesign.se.
Category: Furniture

3. Hazard Information

The product contains perfluorocarboxylic acid related compounds (PFCAs). The total measured value of these substances is up to 0.31 mg/kg. According to the recall notice, these substances bio-accumulate in wildlife and humans, posing a risk to human health and the environment. The product does not comply with the REACH Regulation. The risk type is classified as Chemical and Environment. The level of risk is classified as “Serious risk” in the source data.

4. Consumer Action Required

Consumers who have purchased this product should stop using it immediately. The recall notice specifies that the product has been withdrawn from the market. Consumers are advised to follow the instructions provided by the distributor or importer regarding the return or disposal of the product. No specific consumer action instructions beyond the market withdrawal are detailed in the recall notice.

5. Official Remedy

The following measures have been taken by economic operators:

Distributor: Withdrawal of the product from the market. Date of entry into force: 25/06/2025.
Importer: Withdrawal of the product from the market. Date of entry into force: 12/08/2025.

The recall notice does not specify a refund, replacement, or other consumer-level remedy. The official remedy is the withdrawal of the product from the market by the distributor and importer.

6. Contact Information

Notifying Country: Sweden
EU Safety Gate Alert Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098962
Company Recall Code: Not specified in the recall notice.
Recall URL: Not specified in the recall notice.
Product Images: Available at the following URLs (as provided in the source data):
– https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11009366
– https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11009367

Consumers seeking further information should contact the distributor or importer responsible for the market withdrawal, or refer to the official EU Safety Gate alert page for updates. No direct contact details for the manufacturer or retailer are provided in the recall notice.

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 Cushion?

A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/01524/26).

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

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 Cushion?

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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