Laser engraving machine Recall – EU Safety Gate

Published by Reclia Safety Desk | July 21, 2026

Recall Information Record – Reclia Database

1. Recall Summary
The European Commission Safety Gate alert SR/01544/26, notified by Germany, concerns a Vevor brand laser engraving machine. The product presents a risk of damage to sight due to inadequate safety mechanisms and missing protective shielding. The manufacturer has initiated a recall of the product from end users, and the online marketplace has removed the product listing. The product does not comply with the requirements of the Machinery Directive or European standard EN 60825-1.

2. Affected Products
– Product: Laser engraving machine
– Brand: Vevor
– Type/Model Number: Z3
– Description: Grey/black laser engraver, approximately 15 cm high. Sold online.
– 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: People’s Republic of China
– Notifying Country: Germany
– Case Number: SR/01544/26

3. Hazard Information
The danger identified in the recall notice is that the safety mechanisms are easily bypassed, and the product lacks protective shielding. This allows direct access to laser radiation from the reflected laser beam during operation. Looking directly into the laser beam or exposure via scattered radiation could damage a person’s sight. The risk type is classified as “Damage to sight.” The product does not comply with the Machinery Directive or European standard EN 60825-1.

4. Consumer Action Required
The recall notice specifies that the manufacturer has taken a measure to recall the product from end users. Additionally, the online marketplace has removed the product listing. Consumers who have purchased this product should follow the instructions provided by the manufacturer or the online marketplace regarding the return or disposal of the product. Specific instructions for consumers are not detailed in the recall notice beyond the recall action.

5. Official Remedy
– Type of economic operator taking notified measure(s): Manufacturer
– Category of measure(s): Recall of the product from end users
– Date of entry into force: Unknown
– Type of economic operator taking notified measure(s): Other (online marketplace)
– Category of measure(s): Removal of this product listing by the online marketplace
– Date of entry into force: Unknown

The official remedy is a recall of the product from end users by the manufacturer, and removal of the product listing by the online marketplace. No specific remedy such as refund, replacement, or repair is explicitly stated in the recall notice.

6. Contact Information
– Recall Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099006
– Company Recall Code: Not specified in the recall notice.
– Manufacturer Contact: Not specified in the recall notice.
– Online Marketplace Contact: Not specified in the recall notice.
– Notifying Country Authority: Germany (specific authority contact not provided in the recall notice).

Consumers seeking further information should refer to the Safety Gate alert link above or contact the manufacturer or the online marketplace where the product was purchased. No additional contact details are available in the source data.

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