AIBANA FFP2/KN95
AIBANA FFP2/KN95 was recalled on 4 August 2023 under EU Safety Gate alert A12/01747/23. Health risk / other risk reported by Czechia. The total filtration capacity of the mask is insufficient.
| Alert Number | A12/01747/23 |
| Brand | AIBANA |
| Category | Protective equipment |
| Risk Type | Health risk / other |
| Notifying Country | Czechia |
| Country of Origin | People's Republic of China |
| Published | 4 August 2023 |
Risk Description
The total filtration capacity of the mask is insufficient. Consequently, the product does not fulfil the health and safety requirements and does not properly protect. The product does not comply with the Personal Protective Equipment Regulation nor with the European standard EN 149.
Measures Taken
Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Ban on the marketing of the product and any accompanying measuresDate of entry into force: 22/01/2022Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 22/01/2022
Product Description
Protective respirator in white colour with printed standard and CE marking, missing manufacturer identification, individual pieces in plastic packaging without printing. The product is sold online.
🏥 What Should You Do?
This recall involves a health risk / other hazard related to AIBANA FFP2/KN95.
About this risk
This product poses a health risk that does not fall neatly into a single category. It may involve multiple hazards or an unusual safety concern identified by authorities.
Recommended action
Stop using the product and follow any specific instructions from the recall notice. Contact the manufacturer or your national consumer protection authority for more details.
Who is at risk?
All consumers who have purchased this product.