Particle filter mask Recall – EU Safety Gate

Published by Reclia Safety Desk | July 17, 2026

Here is the factual recall information record based on the provided EU Safety Gate data.

Recall Information Record
Database: Consumer Safety (EU Safety Gate)
Record ID: SR/01337/26
Date of Entry: Based on source data.

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1. Recall Summary

The notifying country, Germany, has issued a recall for a specific model of particle filter mask. The product is identified as an “Atemschutzmaske FFP2 NR” (FFP2 respirator mask) sold under the brand names AHOTOP and LCLEADER. The recall was initiated by the retailer, who has taken measures to withdraw the product from the market and recall it from end users. The product was sold online, particularly via eBay, under the unique product identifier 174608483563.

2. Affected Products

– Product Type: Particle filter mask (FFP2 NR respirator).
– Brand(s): AHOTOP, LCLEADER.
– Product Name: Atemschutzmaske FFP2 NR.
– Model / Type Number: LD-202.
– Description: Coloured FFP2 masks.
– Batch Number: Not specified in the recall notice.
– Barcode: Not specified in the recall notice.
– Country of Origin: People’s Republic of China.
– Distribution: Sold online, in particular via eBay (unique product identifier: 174608483563).
– Production Dates: Not specified in the recall notice.

3. Hazard Information

The recall notice identifies the risk as a “Health risk / other” and classifies it as a “Serious risk.” The specific danger is that the total filtration capacity of the mask is insufficient. Testing has measured the filtration capacity as low as 80%. Consequently, the product does not fulfil the health and safety requirements. The notice states that, even if combined with other recommended measures, the mask may not properly protect the user. The product does not comply with the Personal Protective Equipment (PPE) Regulation nor with the European standard EN 149.

4. Consumer Action Required

Consumers are advised to stop using the affected product immediately. The official measure taken by the retailer includes a recall of the product from end users. Consumers should follow the instructions provided by the retailer regarding the return or disposal of the product. The 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, combined with a withdrawal of the product from the market. The type of economic operator taking the notified measure is the retailer. The date of entry into force for these measures is listed as “Unknown” in the recall notice.

6. Contact Information

– Notifying Country: Germany
– Case Number: SR/01337/26
– EU Safety Gate Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098771
– Retailer Contact: Not specified in the recall notice. Consumers who purchased the product via eBay (unique product identifier: 174608483563) should contact the seller through the eBay platform for specific return or refund instructions.
– Company Recall Code: Not specified in the recall notice.

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