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WARNING LETTER
•Emmons Livestock•September 16, 2022

Emmons Livestock – FDA Warning Letter, Sep 16, 2022

Record Details

On February 10, 2023, the FDA issued a Warning Letter to Mr. Emmons following an inspection of his cattle dealing operation in Maysville, KY, conducted on August 17, September 7, and September 16, 2022. The letter details violations of the Federal Food, Drug, and Cosmetic Act (FD&C Act).

The FDA found that an animal sold for slaughter on December 8, 2021, contained florfenicol at 6.70 ppm and tilmicosin at 1.52 ppm in liver tissue, exceeding the established tolerances of 3.7 ppm and 1.2 ppm, respectively. This renders the food adulterated under 21 U.S.C. § 342(a)(2)(C)(ii). The firm also failed to inquire about the medication status of transported cattle.

Further violations include holding animals under insanitary conditions (21 U.S.C. § 342(a)(4)), such as not cleaning water containers to prevent cross-contamination of medicated and non-medicated liquids. The firm also failed to maintain complete and accurate treatment records, identify and segregate treated cattle, and adequately account for drugs, with several expired drugs found on site.

Additionally, the firm used Increxxa™ (tulathromycin) contrary to label instructions by allowing non-owners/employees

Company
Emmons Livestock
Inspection date
September 16, 2022
Product type
Food
Office
Division of Human and Animal Food Operations - East V
Person
  • Steven Barber (District Director at FDA)
View Company Profile

ID · 20919148-067b-460b-a529-31d1495685c9

Violation Codes9
21 U.S.C. 342(a)(2)(C)(ii)21 U.S.C. 360b(a)(4)(B)21 CFR 556.283(b)(1)(i)21 CFR 556.735(b)(1)(i)21 U.S.C. 342(a)(4)21 CFR 530.11(a)21 U.S.C. 351(a)(5)21 U.S.C. 331(b)21 U.S.C. 331(a)

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