Extension lead Recall – EU Safety Gate

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Published by Reclia Safety Desk | July 21, 2026

📌 EU Safety Gate Recall Notice

Product: Extension lead

Brand: OKKO

Country: Lithuania

Hazards: Chemical Risk, Electric Shock 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/01358/26 |
View original notice →

Recall Summary

Product Extension lead
Brand OKKO
Country Lithuania
Case Number SR/01358/26
Hazard Chemical Risk, Electric Shock Hazard, Non-Compliance
Source 🇪🇺 EU Safety Gate

Recall Information Record – EU Safety Gate Database

Case Number: SR/01358/26
Date of Entry: Not specified in the recall notice.
Notifying Country: Lithuania
Source: EU Safety Gate Weekly Report

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1. Recall Summary

The notifying country of Lithuania has reported a recall for an extension lead sold under the brand OKKO. The product is a three-socket electric extension lead with a cable length of 1.5 metres. The recall was initiated due to a safety defect that presents an electric shock risk to users. The product does not comply with the requirements of the Low Voltage Directive. The measure ordered is the withdrawal of the product from the market. The date of entry into force of the measure is not specified in the recall notice.

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2. Affected Products

– Product type: Extension lead (three socket, 1.5 m cable)
– Brand: OKKO
– Model / Type number: AS-GB03
– Barcode: 4772013039440
– Batch number: Not specified in the recall notice.
– Production dates: Not specified in the recall notice.
– Country of origin: People’s Republic of China
– Importer: The economic operator to whom the measure was ordered is the Importer. The name of the importer is not specified in the recall notice.

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3. Hazard Information

The recall notice identifies the following hazard:

– Risk type: Electric shock
– Nature of the danger: Inadequate protection allows access to live parts. As a result, a user could touch the accessible live parts and receive an electric shock.
– Regulatory non-compliance: The product does not comply with the requirements of the Low Voltage Directive.
– Risk level: The recall notice classifies this as a “Serious risk.”

No other hazards (e.g., chemical risk or fire risk) are explicitly described in the source data. The reference to “Chemical Risk” in the provided summary line is not supported by the body of the recall notice.

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4. Consumer Action Required

The recall notice does not specify any direct consumer action instructions, such as “stop using the product immediately” or “return to the place of purchase.” The only measure described is a regulatory action taken against the economic operator.

What is stated in the source data:
– The measure ordered is: Withdrawal of the product from the market.
– The measure was ordered to the Importer.
– The date of entry into force of the measure is Unknown.

Consumers who have purchased this product should contact the retailer or importer for further guidance. No specific consumer contact procedure is provided in the recall notice.

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5. Official Remedy

The official remedy described in the recall notice is the withdrawal of the product from the market. This means the product is being removed from retail availability to prevent further sales.

The recall notice does not specify a remedy for consumers who already own the product, such as a refund, replacement, or repair. No information is provided regarding whether the importer or retailer will offer a refund or exchange to end users.

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6. Contact Information

– Notifying country authority: Not specified in the recall notice.
– Importer contact details: Not specified in the recall notice.
– Manufacturer contact details: Not specified in the recall notice.
– EU Safety Gate alert reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098868
– Case number: SR/01358/26

Consumers seeking further information should refer to the EU Safety Gate alert page above or contact the retailer where the product was purchased. No direct phone number, email address, or physical address is provided in the recall notice.

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Disclaimer: This record is compiled exclusively from the EU Safety Gate data provided. Any information not present in the source data is noted as “Not specified in the recall notice.” No independent testing, analysis, or opinion has been added.

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 Extension lead?

A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/01358/26).

Q: What should I do if I own the recalled Extension lead?

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 Extension lead?

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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