Laser engraving machine Recall – EU Safety Gate

Published by Reclia Safety Desk | July 17, 2026

Recall Information Record – Reclia Database

1. Recall Summary
The European Commission’s Safety Gate system has published a recall notice concerning a laser engraving machine sold under the brand Vevor. The case number is SR/01544/26, and the notifying country is Germany. The product is classified as machinery and is intended for consumer use. The recall was initiated by the manufacturer and also involves the removal of the product listing by the online marketplace. The date of entry into force for these measures is listed as unknown.

2. Affected Products
– Product: Laser engraving machine
– Brand: Vevor
– Model/Type: Z3
– Description: Grey/black laser engraver, approximately 15 cm high. The product was sold online.
– Country of Origin: People’s Republic of China
– Batch Number: Not specified in the recall notice.
– Barcode: Not specified in the recall notice.
– Production Dates: Not specified in the recall notice.

3. Hazard Information
The recall notice identifies the risk type as “Damage to sight.” The specific danger is described as follows: Because the safety mechanisms are easily bypassed, and because of the lack of a protective shielding, direct access to laser radiation from the reflected laser beam during operation is possible. Looking directly into the laser beam or exposure via scattered radiation could damage a person’s sight. The product does not comply with the requirements of the Machinery Directive or with European standard EN 60825-1.

4. Consumer Action Required
The recall notice states that the manufacturer has taken a measure categorized as “Recall of the product from end users.” Additionally, the online marketplace has taken a measure categorized as “Removal of this product listing by the online marketplace.” The date of entry into force for these measures is listed as unknown. Consumers who have purchased this product should follow the instructions provided by the manufacturer or the online marketplace regarding the recall. Specific instructions for consumers are not detailed in the recall notice beyond the recall measure itself.

5. Official Remedy
The official remedy is a recall of the product from end users, as notified by the manufacturer. The recall notice does not specify whether the remedy includes a refund, replacement, or repair. The online marketplace has also removed the product listing to prevent further sales. No further details on the remedy are provided in the source data.

6. Contact Information
– Notifying Country: Germany
– Case Number: SR/01544/26
– Safety Gate Alert Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099006
– Company Recall Code: Not specified in the recall notice.
– URL for Recall: Not specified in the recall notice.
– Pictures of the product are available at the following URLs:
– https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11010199
– https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11010200
– https://ec.europa.eu/safety-gate-alerts/public/api/notification/image/11010201

Additional Information Not Specified in the Recall Notice:
– The name of the manufacturer or importer.
– A specific telephone number, email address, or website for consumer inquiries.
– The exact date of the recall action.
– Instructions for returning the product or obtaining a refund/replacement.

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