EPA v. Aeris Aair 3-In-1 Pro Air Purifier (COVID-19)

Case summary

The U.S. Environmental Protection Agency, Region 9 (EPA) is informing the Bureau of Customs and Border Protection of the U.S. Department of Homeland Security (CBP) that the following pesticide device import product in the shipment should be Denied Entry Refused Delivery into the United States pursuant to the authority of Section 17(c) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. Section 136o(c), and the implementing regulations at 19 C.F.R. Section 12.114.

Defendants (1)

• Aeris Health, IncNamed in complaintNamed in settlement

Facilities (1)

• AERIS HEALTH INC

  6780 KATELLA AVE., CYPRESS, CA, 90630

  Registry ID: 110071091118

Statutes cited

• FIFRA 12A2N — Failure to File Reports
• FIFRA 12A1F — Device Misbranded

Enforcement conclusions (1)

• Aeris Aair 3-In-1 Pro Air Purifier (COVID-19)entered 2021-10-07

  Primary law: FIFRA

Timeline (3 milestones)

• 2021-10-07Final Order Issued
• 2021-10-07Enforcement Action Closed
• 2021-10-13Enforcement Action Data Entered