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  5. Noel D. Elmore - 11/06/2014
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WARNING LETTER

Noel D. Elmore Nov 06, 2014

Noel D. Elmore - 11/06/2014

Product:
Animal & Veterinary

Recipient:
Noel D. Elmore


United States

Issuing Office:
Cincinnati District Office

United States


   

Department of Health and Human Services logoDepartment of Health and Human Services

Public Health Service
Food and Drug Administration
 
Cincinnati District Office
Central Region
6751 Steger Drive
Cincinnati, OH 45237-3097
Telephone: (513) 679-2700
FAX: (513) 679-2775 

 

WARNING LETTER
CIN-15-442372-07
 
 
November 6, 2014
 
Via United Parcel Service
 
                                                                                                     
Mr. Noel D. Elmore, Owner
Noel Elmore Farms
2310 Woodstore-Etoile Road
Glasgow, Kentucky  42141
 
Dear Mr. Elmore:
 
On August 11, 12 and 15, 2014, the U.S. Food and Drug Administration (FDA) conducted an investigation of your dairy operation located at 2310 Woodstore-Etoile Road, Glasgow, Kentucky. This letter notifies you of the violations of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) that we found during our investigation of your operation. You can find the FD&C Act and its associated regulations on the Internet through links on FDA’s web page at www.fda.gov
 
We found that you offered for sale an animal for slaughter as food that was adulterated. Under section 402(a)(2)(C)(ii) of the FD&C Act, 21 U.S.C. § 342(a)(2)(C)(ii), a food is deemed to be adulterated if it bears or contains a new animal drug that is unsafe under section 512 of the FD&C Act, 21 U.S.C. § 360b. Further, under section 402(a)(4) of the FD&C Act, 21 U.S.C. § 342(a)(4), a food is deemed to be adulterated if it has been held under insanitary conditions whereby it may have been rendered injurious to health.
 
Specifically, our investigation revealed that on or about January 14, 2014, you sold a dairy cow, identified with back tag (b)(4) for slaughter as food.  On or about January 16, 2014, (b)(4) slaughtered this animal. United States Department of Agriculture, Food Safety and Inspection Service (USDA/FSIS) analysis of tissue samples collected from this animal identified the presence of penicillin at 0.215 parts per million (ppm) in the kidney. FDA has established a tolerance of 0.05 ppm for residues of penicillin in the edible tissues of dairy cattle as codified in Title 21, Code of Federal Regulations (C.F.R.), 556.510 (21 C.F.R. 556.510). The presence of this drug in edible tissue from this animal in this amount causes the food to be adulterated within the meaning of section 402(a)(2)(C)(ii) of the FD&C Act, 21 U.S.C. § 342(a)(2)(C)(ii).
 
Our investigation also found that you hold animals under conditions that are so inadequate that medicated animals bearing potentially harmful drug residues are likely to enter the food supply. For example, you failed to maintain complete treatment records, segregate treated animalsand identify treated animals. Food from animals held under such conditions is adulterated within the meaning of section 402(a)(4) of the FD&C Act, 21 U.S.C. § 342(a)(4).
 
The above is not intended to be an all-inclusive list of violations. As a producer of animals offered for use as food, you are responsible for ensuring that your overall operation and the food you distribute is in compliance with the law.
 
You should take prompt action to correct the violations described in this letter and to establish procedures to ensure that these violations do not recur. Failure to do so may result in regulatory action without further notice such as seizure and/or injunction. 
 
Our investigation also revealed that on or about July 5, 2011, you provided (b)(4) with a Livestock Consignor Certification, signed by you, stating that you were not marketing livestock at the (b)(4) with an illegal drug residue. This signed Livestock Consignor Certification covered the dairy cow identified with back tag (b)(4), which was found to have violative levels of penicillin. Providing such a false guaranty is prohibited by section 301(h) of the FD&S Act, 21 U.S.C. 331(h). You should take appropriate actions to ensure that this violation does not recur. 
 
You should notify this office in writing of the steps you have taken to bring your firm into compliance with the law within fifteen (15) working days of receiving this letter. Your response should include each step that has been taken or will be taken to correct the violations and prevent their recurrence. If corrective action cannot be completed within fifteen (15) working days of receiving this letter, state the reason for the delay and the time frame within which the corrections will be completed. Please include copies of any available documentation demonstrating that corrections have been made.
 
Your written response should be sent to Allison C. Hunter, Compliance Officer, U.S. Food and Drug Administration, 6751 Steger Drive, Cincinnati, Ohio 45237. If you have any questions about this letter, please contact Compliance Officer Hunter at 513.679.2700 X2134 or allison. hunter@fda.hhs.gov.
 
Sincerely yours,
/S/ 
Paul Teitell
District Director
Cincinnati District