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WARNING LETTER
•South Central Livestock, Corporation•January 15, 2015

South Central Livestock, Corporation – FDA Warning Letter, Jan 15, 2015

Record Details

On January 8 and 15, 2015, the FDA investigated South Central Livestock Corporation's cattle operation in Lewisburg, Tennessee, and found violations of the Federal Food, Drug, and Cosmetic Act.

A cow sold for slaughter on October 11, 2014, was found to be adulterated. USDA/FSIS analysis of tissue samples from this animal, slaughtered on October 15, 2014, revealed 19.36 ppm of florfenicol in liver tissue (tolerance 3.7 ppm) and 6.99 ppm in muscle tissue (tolerance 0.3 ppm). Additionally, 4.55 ppm of flunixin was found in liver tissue (tolerance 0.125 ppm) and 0.27 ppm in muscle tissue (tolerance 0.025 ppm). These levels exceed established tolerances, rendering the food adulterated under Section 402(a)(2)(C)(ii) of the Act.

The investigation also found insanitary conditions, specifically a failure to maintain treatment records, which could lead to medicated animals with harmful drug residues entering the food supply, violating Section 402(a)(4) of the Act.

Furthermore, the new animal drugs florfenicol (NuflorGold®, NADA # 141-265) and flunixin meglumine (Prevail®,

Company
South Central Livestock, Corporation
Inspection date
January 15, 2015
Product type
Drugs
Office
New Orleans District Office
Person
  • Ruth P. Dixon (Program Division Director)
View Company Profile

ID · 14b3ac3f-2632-4bee-a629-99b18fc9cc11

Violation Codes10
21 U.S.C. 342(a)(2)(C)(i)21 U.S.C. 360b21 U.S.C. 342(a)(4)21 CFR 556.28321 CFR 556.28621 CFR 530.3(a)21 U.S.C. 360b(a)(4)21 U.S.C. 360b(a)(5)21 CFR 53021 CFR 530.11(a)

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