Published by Reclia Safety Desk | July 07, 2026
📌 EU Safety Gate Recall Notice
Product: Laser projector
Brand: Sandowi
Country: Spain
Hazards: Non-Compliance
What to do: Stop using this product. Follow the recall instructions for refund or replacement.
Case #SR/01941/26 |
View original notice →
Recall Summary
| Product | Laser projector |
| Brand | Sandowi |
| Country | Spain |
| Case Number | SR/01941/26 |
| Hazard | Non-Compliance |
| Source | 🇪🇺 EU Safety Gate |
Reclia – Recall Information Database
Record ID: SR/01941/26
Date of Entry: Based on EU Safety Gate data
—
1. Recall Summary
A recall has been issued for the Sandowi brand “Luz de escenario Láser” laser projector. The recall was initiated by authorities in Spain. The product poses a risk of damage to sight due to excessive laser power and improper labelling. The product does not comply with the General Product Safety Regulation nor with the European standards EN 60825-1 and EN 50689. The notifying country is Spain. The country of origin is the People’s Republic of China.
2. Affected Products
– Product: Laser projector (described as a blue laser stage projector)
– Brand: Sandowi
– Name: Luz de escenario Láser
– Type/Model Number: Q-JC20
– Barcode: 8401204820777
– Category: Laser pointers
– Type: Professional
– Batch Number: Not specified in the recall notice.
– Production Dates: Not specified in the recall notice.
– Company Recall Code: Not specified in the recall notice.
3. Hazard Information
The risk type associated with this product is “Damage to sight.” The specific danger identified is that the laser beam is too powerful, with measured values up to 6.9 mW. Additionally, the projector is not properly labelled. Direct viewing of the laser beam could cause damage to sight. The product does not comply with the General Product Safety Regulation nor with the European standards EN 60825-1 and EN 50689. The risk level is classified as “Serious risk.”
4. Consumer Action Required
Consumers are advised to take note of the official measures ordered for this product. The specific instructions for consumers regarding the return or disposal of the product are not detailed in the recall notice. Consumers should refer to the distributor or importer for further guidance on how to proceed.
5. Official Remedy
The following measures have been ordered by the authorities:
– Type of economic operator to whom the measure(s) were ordered: Distributor
– Category of measure(s): Withdrawal of the product from the market
– Date of entry into force: 20/05/2026
– Type of economic operator to whom the measure(s) were ordered: Importer
– Category of measure(s): Withdrawal of the product from the market
– Date of entry into force: 20/05/2026
The official remedy is the withdrawal of the product from the market by both the distributor and the importer. No specific remedy for consumers (such as refund or replacement) is stated in the recall notice.
6. Contact Information
– Notifying Country: Spain
– EU Safety Gate Case Number: SR/01941/26
– EU Safety Gate Reference URL: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099454
– Country of Origin: People’s Republic of China
– Contact details for the distributor or importer: 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 Laser projector?
A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/01941/26).
Q: What should I do if I own the recalled Laser projector?
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 Laser projector?
A: Contact the manufacturer or retailer using the information in the recall notice.
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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.