[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: 9CFR318.24]



[Page 279-281]

 

                  TITLE 9--ANIMALS AND ANIMAL PRODUCTS

 

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

                               AGRICULTURE

 

PART 318_ENTRY INTO OFFICIAL ESTABLISHMENTS; REINSPECTION AND

PREPARATION OF PRODUCTS--Table of Contents

 

                            Subpart A_General

 

Sec. 318.24  Product prepared using advanced meat/bone separation machinery; process control.



    (a) General. Meat, as defined in Sec. 301.2 of this subchapter, may 

be derived by mechanically separating skeletal muscle tissue from the 

bones of livestock, other than skulls or vertebral column bones of 

cattle 30 months of age and older as provided in Sec. 310.22 of this 

subchapter, using advances in mechanical meat/bone separation machinery 

(i.e., AMR systems) that, in accordance with this section, recover 

meat--

    (1) Without significant incorporation of bone solids or bone marrow 

as measured by the presence of calcium and iron in excess of the 

requirements in this section, and

    (2) Without the presence of any brain, trigeminal ganglia, spinal 

cord, or dorsal root ganglia (DRG).

    (b) Process control. As a prerequisite to labeling or using product 

as meat derived by the mechanical separation of skeletal muscle tissue 

from livestock bones, the operator of an establishment must develop, 

implement, and maintain procedures that ensure that the establishment's 

production process is in control.

    (1) The production process is not in control if the skulls entering 

the AMR system contain any brain or trigeminal ganglia tissue, if the 

vertebral column bones entering the AMR system contain any spinal cord, 

if the recovered product fails otherwise under any provision of 

paragraph (c)(1), if the product is not properly labeled under the 

provisions of paragraph (c)(2), or if the spent bone materials are not 

properly handled under the provisions of paragraph (c)(3) of this 

section.

    (2) The establishment must document its production process controls 

in writing. The program must be designed to ensure the on-going 

effectiveness of the process controls. If the establishment processes 

cattle, the program must be in its HACCP plan, its Sanitation SOP,



[[Page 280]]



or other prerequisite program. The program shall describe the on-going 

verification activities that will be performed, including the 

observation of the bones entering the AMR system for brain, trigeminal 

ganglia, and spinal cord; the testing of the product exiting the AMR 

system for bone solids, bone marrow, spinal cord, and DRG as prescribed 

in paragraph (c)(1) of this section; the use of the product and spent 

bone materials exiting the AMR system; and the frequency with which 

these activities will be performed.

    (3) The establishment shall maintain records on a daily basis 

sufficient to document the implementation and verification of its 

production process.

    (4) The establishment shall make available to inspection program 

personnel the documentation described in paragraphs (b)(2) and (b)(3) of 

this section and any other data generated using these procedures.

    (c) Noncomplying product. (1) Notwithstanding any other provision of 

this section, product that is recovered using advanced meat/bone 

separation machinery is not meat under any one or more of the following 

circumstances:

    (i) Bone solids. The product's calcium content, measured by 

individual samples and rounded to the nearest 10th, is more than 130.0 

mg per 100 g.

    (ii) Bone marrow. The product's added iron content, measured by 

duplicate analyses on individual samples and rounded to the nearest 

10th, is more than 3.5 mg per 100 g.\1\

---------------------------------------------------------------------------



    \1\ The excessive iron (ExcFe) measurement for an analyzed sample is 

equal to the obtained iron (Fe) result expressed in mg/100 g measured 

and rounded to the nearest 100th or more for that sample, minus the 

product of three factors: (1) The iron to protein ratio (IPR) factor 

associated with corresponding hand-deboned product; (2) the obtained 

protein (P) result (%) for that sample; and (3) a constant factor of 

1.10. In formula, this can be written as: ExcFe = mFe - IPR x Protein x 

1.10, where ExcFe represents the excess iron, expressed in units of mg/

100 g; mFe represents the measured level of iron (Fe, mg/100 g), IPR is 

the iron to protein ratio for the appropriate hand-deboned product, and 

``Protein'' is the measured level of protein rounded to the nearest 

100th and expressed as a percentage of the total weight of the sample. 

In lieu of data demonstrating otherwise, the values of IPR to be used in 

the above formula are as follows: For beef products the value of IPR is 

equal to 0.104, except for any combination of bones that include any 

beef neckbone product, for which the value of 0.138 is to be used; for 

pork product, the IPR value is 0.052. Other IPR values can be used 

provided that the operator of an establishment has verified and 

documented the ratio of iron content to protein content in the skeletal 

muscle tissue attached to bones prior to their entering the AMR system, 

based on analyses of hand-deboned samples, and the documented value is 

to be substituted for the IPR value (as applicable) in the above formula 

with respect to product that the establishment mechanically separates 

from those bones.

---------------------------------------------------------------------------



    (iii) Brain or trigeminal ganglia. Skulls that enter the AMR system 

have tissues of brain or trigeminal ganglia.

    (iv) Spinal cord. Vertebral column bones that enter the AMR system 

have tissues of spinal cord, or the product that exits the AMR system 

contains spinal cord.

    (v) DRG. The product that exits the AMR system contains DRG.

    (2) If product that may not be labeled or used as ``meat'' under 

this section meets the requirements of Sec. 319.5 of this subchapter, 

it may bear the name ``Mechanically Separated (Species)'' except as 

follows:

    (i) If skulls or vertebral column bones of cattle younger than 30 

months of age that enter the AMR system have tissues of brain, 

trigeminal ganglia, or spinal cord, the product that exits the AMR 

system shall not be used as an ingredient of a meat food product.

    (ii) If product that exits the AMR system contains spinal cord or 

DRG from bones of cattle younger than 30 months of age, it shall not be 

used as an ingredient of a meat food product.

    (iii) If product derived from any bones of cattle of any age does 

not comply with (c)(1)(i) or (ii), it may bear a common or usual name 

that is not false or misleading, except that the product may not bear 

the name ``Mechanically Separated (Beef).''

    (3) Spent skulls or vertebral column bone materials from cattle 

younger than 30 months of age that exit the AMR system shall not be used 

as an ingredient of a meat food product.



[69 FR 1884, Jan. 12, 2004]



[[Page 281]]



Subparts B-F [Reserved]