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Bateman's Mosida Farms LLC MARCS-CMS 484677 —

Animal & Veterinary

Bateman's Mosida Farms LLC

United States

Issuing Office:
Denver District Office

United States


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

Public Health Service
Food and Drug Administration
  Denver District Office
Building 20-Denver Federal Center
P.O. Box 25087
Denver, Colorado 80225-0087
TELEPHONE: 303-236-3000 


January 12, 2016
VIA UPS Overnight
Dr. Robert L. Harding, Owner
Robert L. Harding, DVM Corporation
2279 East 1400 South
Spanish Fork, Utah 84660
Ref: DEN - 16 - 04 - WL
Dear Dr. Harding:
On September 22 and 25, 2015, the U.S. Food and Drug Administration (FDA) conducted an investigation involving the prescribing of drugs in your veterinary practice. Our investigation revealed that you caused the new animal drug (b)(4) (ceftiofur hydrochloride, NADA (b)(4)), to be unsafe under section 512(a)(1) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act), 21 U.S.C. § 360b(a)(1), and adulterated within the meaning of section 501(a)(5) of the FD&C Act, 21 U.S.C. § 351(a)(5), because your practice did not comply with the regulations for  Extralabel Drug Use in Animals, Title 21, Code of Federal Regulations (C.F.R.), Part 530 (21 C.F.R. Part 530). Your actions resulted in an animal being offered for sale for slaughter as food that was 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). 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.
The extra-label use of approved veterinary or human drugs in animals is permitted only if it complies with sections 512(a)(4) and 512(a)(5) of the FD&C Act and 21 C.F.R. Part 530.
Our investigation found that you failed to comply with 21 CFR Part 530 in that you prescribed (b)(4), NADA (b)(4), in an extralabel manner to cattle for difficult calving at (b)(4). Specifically, you prescribed a dose of 25 ml once a day for five days with a withdrawal time of 3 days.  Your dose, indication for use, and withdrawal time were not based on the labeled instructions. You provided treatment protocols to (b)(4) which instruct the staff to treat cattle using (b)(4) for difficult calving, an indication for which this drug is not approved. Also, the treatment protocol you provided included a meat withholding time of 3 days; however, according to the labeled requirements, cattle must not be slaughtered for 4 days following the last treatment with (b)(4). Also, in the protocol you provided to (b)(4), you prescribe the administration of 25 ml (b)(4) once daily over a five day period irrespective of the body weight of the cow, whereas the highest dosage described in the package insert is 2 mL per 100 lbs of body weight. In addition, the protocol does not include instructions to divide the injection amounts over multiple sites; however, labeling for (b)(4) states not to inject more than 15 mL per injection site.
Furthermore, you failed to comply with 21 C.F.R. Part 530 in that you prescribed (b)(4), to be used in an extralabel manner without assuring the use of this drug would not result in a violative drug residue. Specifically, your prescribed extralabel use of this drug in food-producing animals did not meet the requirements of 21 C.F.R. 530.20(a)(2)(ii) and (iv), which require that you:
(ii)     Establish a substantially extended withdrawal period prior to marketing of milk, meat, eggs, or other edible products supported by appropriate scientific information, if applicable; and
(iv)     Take appropriate measures to assure that assigned timeframes for withdrawal are met and no illegal drug residues occur in any food-producing animal subjected to extralabel treatment.
Our investigation also found that your prescription for the extralabel use of (b)(4) resulted in an illegal drug residue in violation of 21 CFR 530.11(d).  Ceftiofur hydrochloride is prohibited for extralabel use in food producing animals by 21 C.F.R. 530.41(a)(13)(ii).
Our investigation also found that your prescription for the extra-label use of (b)(4) did not meet the requirements of 21 C.F.R. 530.12(c), which require that you provide labeling information that shall include the following:
Any directions for use specified by the veterinarian, including the class/species or identification of the animal or herd, flock, pen, lot or other group of animals being treated, in which the drug is intended to be used; the dosage, frequency, and route of administration; and the duration of therapy.
(b)(4) offered a dairy cow, identified with ear tag (b)(4), for slaughter as food that was subsequently found to contain illegal residues in the edible tissue.
Because your use of this drug was not in conformance with its approved labeling and did not comply with 21 CFR Part 530, you caused the drug to be unsafe under section 512(a) of the FD&C Act, 21 U.S.C. § 360b(a), and adulterated within the meaning of section 501(a)(5) of the FD&C Act, 21 U.S.C. § 351(a)(5).
The above is not intended to be an all-inclusive list of violations. As a licensed veterinarian working with animals intended as use for human food, you are responsible for complying with the requirements of the Act, including the extra-label use regulations, including but not limited to ensuring the treatment protocols you distribute are in compliance with the law and applicable approved labeling.
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.
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 Lauren Skokan Priest, Compliance Officer, U.S. Food and Drug Administration, 6th Avenue & Kipling Street – Building 20 DFC, P.O. Box 25087, Denver, Colorado 80225-0087. If you have any questions about this letter, please contact Ms. Priest at (303) 236-9663 or via email at lauren.skokan@fda.hhs.gov.
LaTonya Mitchell
District Director
Denver District
Anna Gallegos
Denver District Manager
PO Box 25387
1 Denver Federal Center
DFC, Building 45 S3
Denver, Colorado 80225
Ms. Luann Adams, Commissioner
Utah Department of Agriculture & Food
350 N. Redwood Road
P.O. Box 146500
Salt Lake City, UT 84414-6500

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