EireMed Respirator Facemask
EireMed Respirator Facemask was recalled on 25 February 2022 under EU Safety Gate alert A12/00339/22. Health risk / other risk reported by Ireland. The particle/filter retention of the material (measured values: as low as 78%) and the total filtration capacity of the mask (measured mean values: as low as 80%) are insufficient.
| Alert Number | A12/00339/22 |
| Brand | EireMed |
| Category | Protective equipment |
| Risk Type | Health risk / other |
| Notifying Country | Ireland |
| Country of Origin | People's Republic of China |
| Model Number | KN95 |
| Published | 25 February 2022 |
Risk Description
The particle/filter retention of the material (measured values: as low as 78%) and the total filtration capacity of the mask (measured mean values: as low as 80%) are insufficient. Consequently, the product does not fulfil 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 nor with the European standard EN 149.
Measures Taken
Type of economic operator taking notified measure(s): ManufacturerCategory of measure(s): Stop of salesDate of entry into force: 09/09/2021
Product Description
White PPE facemasks, branded 'EireMed'. The masks have the CE marking, the claims KN95 and FFP2, and a reference to the European standard EN149 embossed on the side.
🏥 What Should You Do?
This recall involves a health risk / other hazard related to EireMed Respirator Facemask.
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.