94-6242. Ascorbic Acid, Erythorbic Acid, Citric Acid, Sodium Ascorbate, and Sodium Citrate on Beef, Lamb, and Pork Cuts  

  • [Federal Register Volume 59, Number 52 (Thursday, March 17, 1994)]
    [Unknown Section]
    [Page 0]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 94-6242]
    
    
    [[Page Unknown]]
    
    [Federal Register: March 17, 1994]
    
    
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    DEPARTMENT OF AGRICULTURE
    Food Safety and Inspection Service
    
    9 CFR Parts 317 and 318
    
    [Docket No. 89-022F]
    RIN 0583-AB15
    
     
    
    Ascorbic Acid, Erythorbic Acid, Citric Acid, Sodium Ascorbate, 
    and Sodium Citrate on Beef, Lamb, and Pork Cuts
    
    AGENCY: Food Safety and Inspection Service, USDA.
    
    ACTION: Final rule.
    
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    SUMMARY: The Food Safety and Inspection Service (FSIS) is amending the 
    Federal meat inspection regulations to permit the application of 
    ascorbic acid, erythorbic acid, citric acid, sodium ascorbate, and 
    sodium citrate, singly or in combination, to the surface of fresh beef 
    cuts or fresh lamb cuts to delay discoloration of such cuts. Use of 
    these substances will result in the preservation of a fresh color and 
    appearance throughout the product's microbiological shelf life. This 
    action is in response to petitions submitted by Wilson Foods 
    Corporation. In addition, FSIS is amending the regulations to clarify 
    the permitted use and levels of such substances on fresh pork cuts, and 
    revise the purpose of these substances from ``to maintain color'' to 
    ``to delay discoloration'' for clarification. Preserving the fresh 
    color and appearance of beef and lamb cuts increases the marketability 
    of such products; therefore, losses to manufacturers due to color 
    deterioration will be reduced. In addition, FSIS is removing and 
    reserving 9 CFR 317.8(b)(37), which requires qualifying statements on 
    fresh pork cuts.
    
    EFFECTIVE DATE: April 18, 1994.
    
    FOR FURTHER INFORMATION CONTACT:
    Charles R. Edwards, Director, Product Assessment Division, Regulatory 
    Programs, Food Safety and Inspection Service, U.S. Department of 
    Agriculture, Washington, DC 20250, (202) 254-2565.
    
    SUPPLEMENTARY INFORMATION:
    
    Executive Order 12866
    
        This final rule has been reviewed under Executive Order 12866.
    
    Executive Order 12778
    
        This final rule has been reviewed under Executive Order 12778, 
    Civil Justice Reform. States and local jurisdictions are preempted 
    under the Federal Meat Inspection Act (FMIA) from imposing any marking, 
    labeling, packing, or ingredient requirement on federally inspected 
    meat products that are in addition to, or different than, those imposed 
    under FMIA. States and local jurisdictions may, however, exercise 
    concurrent jurisdictions over meat products that are outside official 
    establishments for the purpose of preventing the distribution of meat 
    products that are misbranded or adulterated under the FMIA, or, in the 
    case of imported articles, which are not at such an establishment, 
    after their entry into the United States. Under the FMIA, States that 
    maintain meat inspection programs must impose requirements that are at 
    least equal to those required under the FMIA. The States may, however, 
    impose more stringent requirements on such State inspected products and 
    establishments.
        No retroactive effect will be given to this rule. There are no 
    applicable administrative procedures that must be exhausted prior to 
    any judicial challenge to the provisions of this rule.
    
    Effect on Small Entities
    
        The Administrator, FSIS, has made a determination that this final 
    rule will not have a significant economic impact on a substantial 
    number of small entities. The final rule allows the application of 
    ascorbic acid, erythorbic acid, citric acid, sodium ascorbate, and 
    sodium citrate, singly or in combination, to the surface of fresh beef 
    cuts or fresh lamb cuts to delay discoloration. This final rule will 
    impose no new requirements on small entities. Current regulations 
    already allow these substances to be applied to the surface of fresh 
    pork cuts. Currently, approximately 20 percent to 25 percent of meat 
    packaging companies are producing red meat cuts. FSIS estimates that 
    less than 3 percent of these companies will be affected by this final 
    rule. Also, the Agency estimates the cost of applying these substances 
    to the surface of fresh beef cuts or fresh lamb cuts is between $.03 
    and $.04 per pound. However, if production of fresh beef cuts or fresh 
    lamb cuts treated in this manner increases and a sustained market 
    develops for these products, the cost will decrease.
        The meat industry will benefit from this final action because the 
    preservation of the fresh color and appearance of beef cuts and lamb 
    cuts for a longer period of time should increase the marketability of 
    these products, thereby reducing the losses to manufacturers due to 
    color deterioration of beef cuts and lamb cuts. Manufacturers, both 
    large and small, opting to use such substances will be required to 
    revise the ingredients statement on product labels to show the presence 
    of ascorbic acid, erythorbic acid, citric acid, sodium ascorbate, and/
    or sodium citrate. However, the use of these substances will be 
    voluntary, and any costs associated with new label applications will be 
    covered under existing approved paperwork requirements of FSIS's prior 
    label approval system.
        Manufacturers choosing to apply ascorbic acid, erythorbic acid, 
    citric acid, sodium ascorbate, and sodium citrate, singly or in 
    combination, to fresh beef cuts and fresh lamb cuts will be required to 
    develop and maintain an approved partial quality control (PQC) program, 
    and would thus incur expenses associated with maintaining the PQC 
    program. Decisions by individual manufacturers on whether to use such 
    substances on the surface of fresh beef and fresh lamb cuts will be 
    based on their conclusions that the benefits will outweigh the costs of 
    maintaining the required PQC program. Current regulations already 
    require manufacturers of fresh pork cuts using those substances to 
    develop and maintain an approved PQC program.
    
    Paperwork Requirements
    
        Manufacturers opting to apply ascorbic acid, erythorbic acid, 
    citric acid, sodium ascorbate, or sodium citrate to fresh beef and lamb 
    cuts will be required to develop and maintain a partial quality control 
    (PQC) program. FSIS will receive, evaluate, and either approve or 
    disapprove requests for such PQC programs. The PQC program will be 
    placed on file in the establishment, and be available to any duly 
    authorized representative of the Secretary. The information collection 
    requirements contained in this final rule have been approved by the 
    Office of Management and Budget under approval number 0583-0087.
    
    Background
    
    Wilson Foods Petitions
    
        On December 13, 1988, and October 24, 1991, Wilson Foods 
    Corporation, Oklahoma City, Oklahoma, submitted petitions, along with 
    supporting technical data, to FSIS to permit the application of 
    ascorbic acid, erythorbic acid, sodium ascorbate, citric acid and 
    sodium citrate, singly or in combination, to fresh beef cuts and fresh 
    lamb cuts to delay discoloration of the meat cuts.\1\ The intended 
    effect of ascorbic acid, erythorbic acid, and sodium ascorbate is to 
    serve as antioxidants; the intended effect of citric acid and sodium 
    citrate is to serve as sequestrants. The petitioner's data demonstrate 
    that the required amount to accomplish the intended effects, singly or 
    in combination, would be at levels not to exceed 500 ppm or 1.8 
    milligrams (mg) per square inch of the product's surface of ascorbic 
    acid, erythorbic acid, or sodium ascorbate, and/or not to exceed 250 
    ppm or 0.9 mg per square inch of the product's surface of citric acid 
    or sodium citrate. The data submitted by the petitioner were the 
    results of experiments on products which were packaged in a modified 
    atmosphere of carbon dioxide, oxygen, and nitrogen. It is the Agency's 
    understanding that the benefits provided by the addition of these 
    substances occur regardless of packaging conditions. However, this 
    rulemaking concerns the addition of substances, rather than packaging 
    gases, which are not a part of this rule.
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        \1\Copies of the petitions and supporting technical data are 
    available for review in the FSIS Hearing Clerk's office.
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        The petitioner's data further demonstrate that such treatments 
    result in delaying undesirable discoloration of the product for a 
    period of time that does not exceed the product's microbiological shelf 
    life. Fresh beef cuts and fresh lamb cuts treated with the substances 
    mentioned above and stored at refrigerator temperature will remain 
    wholesome for up to 21 days. Loss of the ``fresh'' color and 
    marketability of beef cuts and lamb cuts occurs before the product 
    becomes microbiologically unsafe. Some consumers are reluctant to 
    purchase fresh beef or lamb cuts because of the change to a darker 
    color of the product before spoilage.
    
    Current Regulations
    
        Section 318.7(c)(4) of the Federal meat inspection regulations (9 
    CFR 318.7(c)(4)) allows the use of ascorbic acid, erythorbic acid, 
    citric acid, sodium ascorbate, and sodium citrate on fresh pork cuts to 
    maintain color at levels not to exceed either 500 ppm or 1.8 mg/sq inch 
    of surface of ascorbic acid, erythorbic acid or sodium ascorbate, 
    singly or in combination, and/or not to exceed either 250 ppm or 0.9 
    mg/sq inch of surface of citric acid or sodium citrate, singly or in 
    combination. In addition, 9 CFR 318.7(c)(4) requires the use of such 
    substances under an approved PQC program under 9 CFR 318.4(d) and (e). 
    Section 317.8(b)(37) of the Federal meat inspection regulations (9 CFR 
    317.8(b)(37)) requires that when ascorbic acid, erythorbic acid, citric 
    acid, sodium ascorbate, and sodium citrate, singly or in combination, 
    are added to fresh pork cuts, there shall appear on the label of that 
    product, in letters of the same style and type and not less than one-
    fourth the size of letters in the product name, contiguous to the name 
    of the product, a statement identifying the specific approved 
    substance(s) by its common name and the purpose for which it is added 
    such as ``Sprayed with a solution of water, ascorbic acid and citric 
    acid to maintain color.''
        The Food and Drug Administration (FDA) lists ascorbic acid in 21 
    CFR 182.3013, erythorbic acid in 21 CFR 182.3041, and sodium ascorbate 
    in 21 CFR 182.3731 as generally recognized as safe (GRAS) when used in 
    accordance with good manufacturing practices for use as preservatives. 
    FDA lists citric acid in 21 CFR 182.6033 and sodium citrate in 21 CFR 
    182.6751 as GRAS when used in accordance with good manufacturing 
    practices for use as sequestrants.
    
    Proposed Rule
    
        On October 4, 1993, FSIS published a proposed rule in the Federal 
    Register (58 FR 51581) to permit the application of ascorbic acid, 
    erythorbic acid, citric acid, sodium ascorbate, and sodium citrate, 
    singly or in combination, to the surface of fresh beef cuts or fresh 
    lamb cuts to delay discoloration of such meat cuts. The proposed rule 
    would allow these substances to be used, singly or in combination, at 
    levels of not more than 500 ppm or 1.8 milligrams per square inch of 
    product surface area for ascorbic acid, erythorbic acid or sodium 
    ascorbate, and/or not more than 250 ppm or 0.9 milligrams per square 
    inch of surface area for citric acid or sodium citrate to achieve the 
    intended technical effects.
        FSIS also proposed that processors who apply these substances to 
    cuts of fresh beef and lamb be required to follow an approved PQC 
    program as set forth in 9 CFR 318.4(d). Neither processing of such 
    products nor distribution of such products in commerce would be 
    permitted until such PQC programs are approved and utilized according 
    to the requirements set forth in 9 CFR 318.4(e). All such PQC programs 
    would cover certain critical control points, including: (1) The 
    condition of the meat before treatment (it must be fresh or previously 
    frozen and maintained in a wholesome condition, evidenced by time and 
    temperature records from the point of slaughter), (2) solution 
    formulation control, (3) single application control, (4) finished 
    product ingredient analysis monitoring, and (5) integrity of the 
    packaging during storage, transportation, and distribution. This would 
    ensure that these substances applied to the surface of the meat cuts to 
    delay discoloration would not be applied in excessive amounts; 
    therefore, the discoloration of the cuts would occur before the onset 
    of microbiological spoilage.
        Cuts of fresh pork treated with ascorbic acid, erythorbic acid, 
    sodium ascorbate, sodium citrate, and citric acid are currently 
    required by 9 CFR 317.8(b)(37) to be labeled with a statement 
    identifying these substances by their common and usual name and the 
    purpose for which they are used; e.g., ``Sprayed with a solution of 
    water, ascorbic acid and citric acid to maintain color.'' This 
    statement is required to be shown on the label in a prominent manner, 
    contiguous to the product name, in letters of the same style and type 
    and not less than one-fourth the size of the largest letter in the 
    product name. After reassessing its overall policy regarding prominent 
    labeling, FSIS set forth in the proposed rule that 9 CFR 317.8(b)(37) 
    requiring qualifying statements on fresh pork cuts would be removed and 
    reserved.
        In addition, on November 4, 1992, the Agency published in the 
    Federal Register a proposed rule (57 FR 52596) to eliminate those 
    prominent disclosure requirements for product name qualifiers where the 
    inclusion of a substance does not significantly alter the basic 
    identity of the finished product or where the prominently disclosed 
    information can be found in the ingredients statement. Such rule, in 
    part, would eliminate product name qualifiers on fresh pork cuts 
    treated with ascorbic acid, erythorbic acid, sodium ascorbate, sodium 
    citrate, and citric acid. FSIS is considering the publication of a 
    final rule on prominent labeling which would become effective in the 
    near future. FSIS believes that such action would not deprive consumers 
    of informative labeling because all substances used in the preparation 
    of a product are required to be listed in the ingredients statement (9 
    CFR 317.2(f)(1)). However, as indicated in the proposed rule on 
    ascorbic acid and other substances, FSIS is removing and reserving 9 
    CFR 318.7(b)(37). Therefore, as of the effective date of this final 
    rule, qualifying statements, which identify the presence of ascorbic 
    acid, erythorbic acid, sodium ascorbate, sodium citrate, and citric 
    acid on fresh port cuts, are no longer required on the labeling of 
    fresh pork cuts which contain such substances.
        FSIS also stated in the preamble to the proposed rule that 9 CFR 
    317.8(b)(6) prohibits the word ``fresh'' on labels to designate product 
    which has been salted for preservation. Therefore, FSIS would not allow 
    the word ``fresh'' to be used on the labels of products treated with 
    ascorbic acid, erythorbic acid, sodium ascorbate, sodium citrate, and 
    citric acid.
        FSIS proposed to amend the table of approved substances in 9 CFR 
    318.7 by revising the current entry for the Class of substance titled 
    ``Miscellaneous,'' under the Substance column for ``Ascorbic, 
    erythorbic acid, citric acid, sodium ascorbate, and sodium citrate'' to 
    include such use on fresh beef and lamb cuts, along with the existing 
    use on fresh pork cuts. In addition, FSIS proposed that the entry be 
    revised to clarify the permitted use and levels of such substances on 
    fresh pork cuts. The Agency also proposed to revise the purpose of 
    these substances from ``to maintain color'' to ``to delay 
    discoloration'' for clarification.
    
    Discussion of Comments
    
        FSIS received three comments in response to the proposed rule. The 
    comments were submitted by a consultant and two food manufacturers. The 
    commenters fully supported the proposed rule.
        After review of the comments and other information, the 
    Administrator has determined that the application of ascorbic acid, 
    erythorbic acid, citric acid, sodium ascorbate, and sodium citrate to 
    the surface of fresh beef and lamb cuts, as permitted in the rule, will 
    not render the products in which they are used adulterated or 
    misbranded or otherwise not in compliance with the Federal Meat 
    Inspection Act. The Administrator has further determined that these 
    substances will be functional and suitable for the products and will be 
    permitted for use on the surface of fresh beef and lamb cuts as the 
    lowest level necessary to accomplish the stated technical effect.
    
    List of Subjects
    
    9 CFR Part 317
    
        Meat inspection, Food labeling.
    
    9 CFR Part 318
    
        Meat inspection, Food additives.
    
    Final Rule
    
        For reasons discussed in the preamble, FSIS is amending 9 CFR parts 
    317 and 318 of the Federal meat inspection regulations as follows:
    
    PART 317--LABELING, MARKING DEVICES, AND CONTAINERS
    
        1. The authority citation for part 317 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 601-695; 7 CFR 2.17, 2.55.
    
        2. Section 317.8 is amended by removing and reserving paragraph 
    (b)(37).
    
    PART 318--ENTRY OFFICIAL ESTABLISHMENTS; REINSPECTION AND 
    PREPARATION OF PRODUCTS
    
        3. The authority citation for part 318 continues to read as 
    follows:
    
        Authority: 7 U.S.C. 450, 1901-1906; 21 U.S.C. 601-695; 7 CFR 
    2.17, 2.55.
    
        4. In the table in Sec. 318.7(c)(4) under the Class of substance 
    ``Miscellaneous,'' the entry under the Substance ``Ascorbic Acid, 
    erythorbic acid, citric acid, sodium ascorbate, and sodium citrate'' is 
    revised to read as follows:
    
    
    Sec. 318.7  Approval of substances for use in the preparation of 
    products.
    
    * * * * *
        (c) * * *
        (4) * * *
    
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     Class of substance        Substance              Purpose               Product                  Amount         
    ----------------------------------------------------------------------------------------------------------------
                                                                                                                    
                                                                                                                    
                                                      * * * * * * *                                                 
    Miscellaneous.......  Ascorbic acid,        To delay              Fresh beef cuts,      Not to exceed, singly or
                           erythorbic acid,      discoloration.        fresh lamb cuts,      in combination, 500 ppm
                           citric acid, sodium                         and fresh pork cuts.  or 1.8 mg/sq inch of   
                           ascorbate and                                                     product surface of     
                           sodium citrate,                                                   ascorbic acid (in      
                           singly or in                                                      accordance with 21 CFR 
                           combination, under                                                182.3013), erythorbic  
                           an approved partial                                               acid (in accordance    
                           quality control                                                   with 21 CFR 182.3041), 
                           (PQC) program (9                                                  or sodium ascorbate (in
                           CFR 318.4 (d) &                                                   accordance with 21 CFR 
                           (e)).                                                             182.3731); and/or not  
                                                                                             to exceed, singly or in
                                                                                             combination, 250 ppm or
                                                                                             0.9 mg/sq inch of      
                                                                                             product surface of     
                                                                                             citric acid (in        
                                                                                             accordance with 21 CFR 
                                                                                             182.6033), or sodium   
                                                                                             citrate (in accordance 
                                                                                             with 21 CFR 182.6751). 
                                                                                                                    
                                                                                                                    
                                                      * * * * * * *                                                 
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        Done at Washington, DC, on: March 11, 1994.
    Patricia Jensen,
    Acting Assistant Secretary, Marketing & Inspection Services.
    [FR Doc. 94-6242 Filed 3-16-94; 8:45 am]
    BILLING CODE 3410-DM-M
    
    
    

Document Information

Published:
03/17/1994
Department:
Food Safety and Inspection Service
Entry Type:
Uncategorized Document
Action:
Final rule.
Document Number:
94-6242
Dates:
April 18, 1994.
Pages:
0-0 (1 pages)
Docket Numbers:
Federal Register: March 17, 1994, Docket No. 89-022F
RINs:
0583-AB15
CFR: (1)
9 CFR 318.7