Herbal product for smoking Recall – EU Safety Gate

Published by Reclia Safety Desk | July 21, 2026

Recall Information Record – Reclia Database

1. Recall Summary
This recall notice, case number SR/01973/26, was issued by the notifying country of Czechia on 21 May 2026. The product is a herbal product intended for smoking, sold under the brand name ECOCANNA and the product name “Cyborg.” The recall was initiated due to the presence of a psychoactive cannabinoid (MDMB-PINACA) in the product, which poses a serious chemical risk to consumers. The product does not comply with the General Product Safety Regulation. The measure ordered is the withdrawal of the product from the market by the retailer.

2. Affected Products
– Product type: Herbal product for smoking
– Brand: ECOCANNA
– Product name: Cyborg
– Type/Model number: 1g
– Batch number: Not specified in the recall notice
– Barcode: 8591193960315
– Country of origin: Unknown
– Production dates: Not specified in the recall notice
– Company recall code: Not specified in the recall notice
– Distribution: The product was available for sale in Czechia. The specific retail locations or online platforms where the product was sold are not specified in the recall notice.

3. Hazard Information
The product contains a psychoactive cannabinoid identified as MDMB-PINACA. According to the recall notice, this substance is a highly potential psychoactive substance that acts on the central nervous system. The use of this substance is associated with the risk of serious toxic effects, including:
– Acute intoxication
– Impaired consciousness
– Mental and behavioral disorders
– Neurological complications
– Cardiovascular effects

The recall notice classifies the risk level as “Serious risk.” The product does not comply with the General Product Safety Regulation. No other hazard types (such as laceration hazard) are explicitly described in the source data; the only hazard listed in the source data is the chemical risk from the psychoactive cannabinoid.

4. Consumer Action Required
The recall notice does not provide specific instructions directed at consumers. The measure ordered is the withdrawal of the product from the market by the retailer. Consumers who have purchased this product should stop using it immediately. Based on the official measure, consumers should return the product to the place of purchase or contact the retailer for further instructions. No specific consumer contact or return procedure is detailed in the recall notice.

5. Official Remedy
The official remedy ordered by the notifying authority is the withdrawal of the product from the market. The type of economic operator to whom the measure was ordered is the retailer. The date of entry into force of the measure is 21 May 2026. No information regarding a refund, replacement, or other compensation for consumers is explicitly stated in the recall notice.

6. Contact Information
– Notifying country: Czechia
– Case number: SR/01973/26
– Reference link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099388
– Retailer contact information: Not specified in the recall notice
– Manufacturer contact information: Not specified in the recall notice
– Consumer hotline or email: Not specified in the recall notice

Consumers seeking further information should refer to the official EU Safety Gate alert using the reference link above or contact the relevant consumer protection authority in Czechia. No additional contact details are provided in the source data.

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