[Code of Federal Regulations]

[Title 9, Volume 2]

[Revised as of January 1, 2007]

From the U.S. Government Printing Office via GPO Access

[CITE: 9CFR309.16]



[Page 111-113]

 

                  TITLE 9--ANIMALS AND ANIMAL PRODUCTS

 

     CHAPTER III--FOOD SAFETY AND INSPECTION SERVICE, DEPARTMENT OF 

                               AGRICULTURE

 

PART 309_ANTE-MORTEM INSPECTION--Table of Contents

 

Sec. 309.16  Livestock suspected of having biological residues.



    (a) Except as provided by paragraph (d) of this section, livestock 

suspected of having been treated with or exposed to any substance that 

may impart a biological residue which would make the edible tissues 

unfit for human food or otherwise adulterated shall be handled in 

compliance with the provisions of this paragraph. They shall be 

identified at official establishments as ``U.S. Condemned.'' These 

livestock may be held under the custody of a Program employee, or other 

official designated by the Administrator, until metabolic processes have 

reduced the residue sufficiently to make the tissues fit for human food 

and otherwise not adulterated. When the required time has elapsed, the 

livestock, if returned for slaughter, must be re-examined on ante-mortem 

inspection. To aid in determining the amount of residue present in the 

tissues, officials of the Program may permit the slaughter of any such 

livestock for the purpose of collecting tissues for analysis for the 

residue. Such analysis may include the use of inplant screening 

procedures designed to detect the presence of antimicrobial residues in 

any species of livestock.

    (b) All carcasses and edible organs and other parts thereof, in 

which are found any biological residues which render such articles 

adulterated, shall be marked as ``U.S. Condemned'' and disposed of in 

accordance with Sec. 314.1 or Sec. 314.3 of this chapter.

    (c) [Reserved]

    (d) Calves shall not be presented for ante-mortem inspection in an 

official establishment except under the provisions of this paragraph.

    (1) Definitions. For purposes of this paragraph, the following 

definitions shall apply:

    (i) Calf. A calf up to 3 weeks of age or up to 150 pounds.

    (ii) Certified calf. A calf that the producer and all other 

subsequent custodians of the calf certify in writing has not been 

treated with any animal drug while in his or her custody or has



[[Page 112]]



been treated with one or more drugs in accordance with FDA approved 

label directions while in his or her custody and has been withheld from 

slaughter for the period(s) of time specified by those label directions.

    (iii) Healthy calf. A calf that an inspector determines shows no 

visual signs of disease or treatment of disease at ante-mortem 

inspection.

    (iv) Producer. The owner of the calf at the time of its birth.

    (v) Sick calf. A calf that an inspector on ante-mortem inspection 

determines has either signs of treatment or signs of disease.

    (vi) Veterinary medical officer. An inspector of the Program that 

has obtained a Doctor of Veterinary Medicine degree which is recognized 

by the Program.

    (2) General requirements. (i) The identity of the producer of each 

calf presented for ante-mortem inspection shall be made available by the 

official establishment to the inspection prior to the animal being 

presented for ante-mortem inspection.

    (ii) The inspector shall segregate the calves presented for ante-

mortem inspection at the establishment and identify each calf as one of 

the following: (a) Certified, (B) noncertified, or (C) previous residue 

condemnation.

    (3) Certified group. (i) For a calf to be considered certified, the 

producer and all other subsequent custodians of the calf must certify in 

writing that while the calf was in his or her custody, the calf was not 

treated with animal drugs or was treated with one or more drugs in 

accordance with FDA approved label directions and was withheld from 

slaughter for the period(s) of time specified by those label directions. 

All prior certifications must be presented with the animal at the time 

of slaughter. The certifications shall contain a list of the calves with 

accompanying identification numbers, as required by paragraph (d)(3)(ii) 

of this section, followed by the following language:



    I hereby certify that, while in my custody, from -------- to ------

-- (time period of custody), the above-listed calf or calves have not 

been treated with drugs, or have been treated with one or more drugs in 

accordance with FDA approved label directions and have been withheld 

from slaughter for the period(s) of time specified by those label 

directions. I certify that, to the best of my knowledge and belief, all 

information contained herein is true, that the information may be relied 

upon at the official establishment, and that I understand that any 

willful falsification of this certification is a felony and may result 

in a fine of up to $250,000 for an individual or up to $500,000 for an 

organization, or imprisonment for not more than 5 years, or both (21 

U.S.C. 677, 18 U.S.C. 1001 and 3571).



Executed on_____________________________________________________________

 (date of certification)



[fxsp0]_________________________________________________________________

(signature of certifier)



[fxsp0]_________________________________________________________________

(typed or printed name and address of certifier)



[fxsp0]_________________________________________________________________

(business of certifier)



    (ii) Each calf must be identified by use of backtag, eartag, or 

other type of secure identification which displays a number which shall 

be recorded on all written certifications.

    (iii) The inspector shall have segregated for veterinary medical 

officer examination any certified calf which he or she determines to 

show any sign of disease or which is not identified individually. Such 

animal will be tagged as ``U.S. Suspect'' and its carcass will be 

retained on post-mortem inspection and handled in accordance with Sec. 

310.21 (c) and (d).

    (iv) The inspector shall handle the remaining carcasses of healthy 

animals in accordance with Sec. 310.21(c) and (d).

    (4) Noncertified group. On ante-mortem inspection, the inspector 

shall have segregated for veterinary medical officer examination any 

calf which he or she determines to show any sign of disease. Such animal 

will be tagged as ``U.S. Suspect'' and its carcass will be retained on 

post-mortem inspection and handled in accordance with Sec. 310.21(c). 

The inspector shall handle the remaining carcasses of healthy animals in 

accordance with Sec. 310.21(c).

    (5) Calves from producers with previous residue condemnation. On 

ante-mortem inspection, the inspector shall have segregated for 

veterinary medical officer examination any calf which he or she 

determines to show any sign of disease. Such animal will be tagged as 

``U.S. Suspect'' and its carcass will be retained on post-mortem 

inspection and handled in accordance with



[[Page 113]]



Sec. 310.21(e). The inspector shall handle the remaining carcasses of 

healthy animals in accordance with Sec. 310.21(e).

    (e) The name of each and all person(s) who sold or consigned each 

swine to the establishment shall be made available by the establishment 

to any Program employee or other authorized employee of the United 

States Department of Agriculture upon that employee's request and 

presentation of his or her official credentials. Swine identification, 

by means approved by the Animal and Plant Health Inspection Service, 

USDA, under part 71 of this title, must be maintained throughout post-

mortem inspection, in accordance with Sec. 310.23(a) of this 

subchapter.



(Recordkeeping requirements approved by the Office of Management and 

Budget under control number 0583-0053)



[36 FR 24928, Dec. 24, 1971, as amended at 44 FR 45606, Aug. 3, 1979; 44 

FR 59499, Oct. 16, 1979; 47 FR 746, Jan. 7, 1982; 47 FR 41336, Sept. 20, 

1982; 50 FR 32164, Aug. 9, 1985; 50 FR 53127, Dec. 30, 1985; 52 FR 2104, 

Jan. 20, 1987; 53 FR 40387, Oct. 14, 1988; 55 FR 7474, Mar. 2, 1990]