PUREMEN KN95
PUREMEN KN95 was recalled on 29 April 2022 under EU Safety Gate alert INFO/00089/22. Health risk / other risk reported by Germany. The product bears a CE marking but its filtering capacity has not been tested by a relevant competent European conformity assessment body.
| Alert Number | INFO/00089/22 |
| Brand | PUREMEN |
| Category | Protective equipment |
| Risk Type | Health risk / other |
| Notifying Country | Germany |
| Country of Origin | People's Republic of China |
| Model Number | KN95 MASk-001 |
| Published | 29 April 2022 |
Risk Description
The product bears a CE marking but its filtering capacity has not been tested by a relevant competent European conformity assessment body. Consequently, it is not proven that the product fulfils the health and safety requirements; thus, even if combined with other recommended measures, it may not properly protect. The product does not comply with the Personal Protective Equipment Regulation and with the European standard EN 149.
Measures Taken
Type of economic operator taking notified measure(s): RetailerCategory of measure(s): Stop of sales at all locationsDate of entry into force: 03/02/2022
Product Description
Protective respiratory filtration half-face mask. The mask is marked with both FFP2 and KN95 indications, and has the CE marking printed on the side.
🏥 What Should You Do?
This recall involves a health risk / other hazard related to PUREMEN 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.