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  5. Gordondale Farms, Inc. - 02/24/2016
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Gordondale Farms, Inc.

Animal & Veterinary

Gordondale Farms, Inc.

United States

Issuing Office:
Minneapolis District Office

United States


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

Public Health Service
Food and Drug Administration
Minneapolis District Office
Central Region
250 Marquette Avenue, Suite 600
Minneapolis, MN 55401
Telephone: (612) 334-4100
FAX: (612) 334-4142 


February 24, 2016
Via UPS Overnight Delivery                                           
Refer to MIN 16 - 07
Kyle D. Gordon
Gordondale Farms, Inc.
P.O. Box 26
Nelsonville, Wisconsin 54458-0026
Dear Mr. Gordon:
On February 4 and 5, 2016, the U.S. Food and Drug Administration (FDA) conducted an investigation of your dairy operation located at 9845 Highway 161, Amherst Junction, Wisconsin.  This letter notifies you of violations of the Federal Food, Drug, and Cosmetic Act (the Act) that we found during our investigation of your operation.  You can find the 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 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 Act, 21 U.S.C. § 360b.  Further, under section 402(a)(4) of the 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 August 25, 2015, you sold a dairy cow identified with backtag #(b)(4), corresponding to your farm ear tag #(b)(4), for slaughter as food.  On or about August 26, 2016, (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 desfuroylceftiofur (marker residue for ceftiofur) at 0.54 parts per million (ppm) in kidney tissue. The FDA has established a tolerance of 0.4 ppm desfuroylceftiofur in the kidney tissue of cattle, as codified in Title 21, Code of Federal Regulations (CFR), section 556.113(b)(3)(i), (21 CFR 556.113(b)(3)(i)). 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 Act, 21 U.S.C. § 342(a)(2)(C)(ii).
Our investigation also found that you hold animals under conditions that fail to prevent medicated animals bearing potentially harmful drug residues from entering the food supply.  For example, you failed to have an adequate system to verify the entry of written treatment records into your electronic treatment records to ensure that meat and milk withhold times are met. Food from animals held under such conditions is adulterated within the meaning of section 402(a)(4) of the 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 are 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.
During a 2014 FDA investigation of a tissue residue violation at your operation, you stated that undocumented use of drugs by a herdsman was the most likely cause of these tissue residue violations.  Following that determination, you relieved that herdsman of his duties at your farm.  In early 2013, a similar issue with a herdsman contributed to another drug residue.  These recurring residues may indicate a problem with your practices for hiring, training, and/or supervising herdsmen.
Please notify this office in writing of the steps you have taken to bring your firm into compliance with the law within 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 15 working days of receiving this letter, state the reason for the delay and the timeframe 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 Brian D. Garthwaite, Ph.D., Compliance Officer, at the address listed on this letterhead.  If you have any questions about this letter, please contact Dr. Garthwaite at (612) 758-7132.
Michael Dutcher, DVM
Minneapolis District
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