USDA Updates Paperwork Rules for Private Cow Quarantines
Published Date: 5/22/2026
Notice
Summary
The USDA wants to update and keep collecting info from privately owned quarantine facilities that care for ruminants like cows and deer. This affects facility owners who must follow new rules to keep animals safe and healthy. Comments on these changes are open until July 21, 2026, and the update helps protect animals without adding big costs.
Analyzed Economic Effects
3 provisions identified: 0 benefits, 3 costs, 0 mixed.
30-Day Quarantine Requirement for Imports
Ruminants imported into the United States must be quarantined upon arrival for at least 30 days, with certain exceptions. Ruminants from Canada and Mexico are not subject to this quarantine requirement.
New Quarantine Facility Paperwork Rules
If you own or operate a privately owned quarantine facility for ruminants, you must use specified information collections: an application for facility approval, a cooperative service (compliance) agreement, a daily log of persons entering and leaving during quarantine, requests for variances, a manual of standard operating procedures, and maintenance of quarantine records. APHIS cites these activities under 9 CFR part 93, subpart D and is seeking OMB approval (OMB Control Number 0579-0232) to continue collecting this information.
Estimated Paperwork Burden and Scope
APHIS estimates the average burden is 0.604 hours per response. The agency estimates 2 respondents (owners/operators), 53 responses per respondent, 106 total annual responses, and 64 total annual burden hours; APHIS requests approval for an additional 3 years and will accept comments through July 21, 2026.
Your PRIA Score
Personalized for You
How does this regulation affect your finances?
Sign up for a PRIA Policy Scan to see your personalized alignment score for this federal register document and every other regulation we track. We analyze your financial profile against policy provisions to show you exactly what matters to your wallet.
Key Dates
Department and Agencies
Related Federal Register Documents
2026-13238 — Soil Culture Solutions, LLC: Determination of Nonregulated Status of HLB-Resistant Carrizo Citrange Rootstock (CarriCea T1)
The USDA says Soil Culture Solutions’ genetically engineered Carrizo citrange rootstock, called CarriCea T1, is safe and no longer needs special regulation. This rootstock fights citrus greening disease, helping farmers protect their citrus trees starting June 30, 2026. Growers can now use this disease-resistant rootstock without extra paperwork or fees, making citrus farming easier and more affordable.
2026-13285 — Notice of Request for Revision to and Extension of Approval of an Information Collection; Virus-Serum-Toxin Act and Regulations
The USDA’s Animal and Plant Health Inspection Service (APHIS) wants to update and keep collecting info related to the Virus-Serum-Toxin Act, which helps keep animal medicines safe. This affects companies making or shipping vaccines and similar products. They’re asking for public comments by August 31, 2026, and there’s no new cost announced—just a smooth continuation with some tweaks.
2026-13043 — Notice of Request for Revision to and Extension of Approval of an Information Collection; Importation of Swine Hides, Bird Trophies, and Deer Hides
The USDA’s Animal and Plant Health Inspection Service wants to keep collecting info on importing swine hides, bird trophies, and deer hides, with some updates to the process. This affects businesses and people who bring these items into the U.S., and they’re asking for public feedback by August 28, 2026. No big cost changes are expected, but staying in the loop helps keep imports safe and smooth.
2026-12243 — Notice of Request for Revision to and Extension of Approval of an Information Collection; African Swine Fever; Importation of Live Dogs for Resale From Regions Where ASF Exists or Is Reasonably Believed To Exist
The USDA is updating and extending rules about importing live dogs for resale from places where African Swine Fever (ASF) is known or suspected. This affects dog importers who must provide updated info to help keep ASF out of the U.S. You’ve got until August 17, 2026, to share your thoughts, and these changes aim to keep things safe without adding big costs.
2026-12242 — Notice of Intent To Prepare a Programmatic Environmental Impact Statement; Grasshopper and Mormon Cricket Suppression Program
The USDA’s Animal and Plant Health Inspection Service is updating its plan to control grasshoppers and Mormon crickets across 17 western states. They’re asking the public to share ideas and concerns by July 20, 2026, before finalizing the plan in August 2027. This effort aims to protect rangelands and farming without causing harm to the environment or people.
2026-11644 — Notice of Request for Revision to and Extension of Approval of an Information Collection; Importation of Table Eggs From Regions Where Newcastle Disease or Highly Pathogenic Avian Influenza Is Considered to Exist and Exportation of Poultry and Hatching Eggs
The USDA is updating and extending the paperwork rules for importing table eggs from places with bird diseases like Newcastle disease and avian flu, and for exporting poultry and hatching eggs from the U.S. This affects farmers, egg importers, and exporters who’ll need to follow the revised info collection. Comments on these changes are open until August 10, 2026, with no new fees announced.
Previous / Next Documents
Previous: 2026-10291 — Environmental Impact Statements; Notice of Availability
The EPA just shared new Environmental Impact Statements (EIS) for projects like oil drilling and lab upgrades in California and Oregon. If you’re involved in these areas, you’ve got until June 22, 2026, to check out the details and share your thoughts. These reviews help protect the environment while balancing development, with no immediate costs but big future benefits.
Next: 2026-10295 — M11 Clinical Electronic Structured Harmonised Protocol (CeSHarP); International Council for Harmonisation; Guidance for Industry; Availability
The FDA just released a new, easy-to-use digital guide called M11 CeSHarP to help everyone involved in clinical trials share and review study plans faster and clearer. This affects drug companies, researchers, and regulators worldwide by setting a global standard for how trial info is written and shared electronically. The new rules kick in now, aiming to save time and reduce confusion, with no direct cost but big efficiency gains.