EPA v. Molecure - UV Room Sterilizer (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 eight (8) pesticide device products in the shipment described below 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)

• Molecure IncNamed in complaintNamed in settlement

Facilities (1)

• MOLECURE INC.

  2 PARK AVE 20TH FLOOR, NEW YORK, NY, 10016

  Registry ID: 110070890786

Statutes cited

• FIFRA 12A2L — Establishment Registration
• FIFRA 12A2N — Failure to File Reports
• FIFRA 12A1F — Device Misbranded

Enforcement conclusions (1)

• Molecure - UV Room Sterilizer (COVID-19)entered 2020-10-02

  Primary law: FIFRA

Timeline (3 milestones)

• 2020-10-02Enforcement Action Closed
• 2020-10-02Final Order Issued
• 2021-02-03Enforcement Action Data Entered