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    過敏原Guidance on Inspections of Firms Producing Food

    放大字體  縮小字體 發(fā)布日期:2005-06-18  來源:食品論壇 菩提樹

    August 2001

    This guidance is reference material for investigators and other FDA personnel. The guidance

    does not bind FDA and does not confer any rights, privileges, benefits or immunities for or

    on any person(s). An alternative approach may be used if such an approach satisfies the

    requirements of the applicable statutes, regulations, or both.

    FDA has developed inspection guidance identifying the following areas in the manufacture ofg

    foods that may result in undeclared food allergens: 1) Products that contain one or more allergenic

    ingredients, but the label does not declare the ingredient in the ingredient label; 2) Products that

    become contaminated with an allergenic ingredient due to the firm’s failure to exercise adequate

    control procedures; 3) Products that are contaminated with an allergenic ingredient due to the

    nature of the product or process; 4) Products that contain a flavor ingredient that has an allergenic

    component, but the label of the product only declares the flavor; and 5) Products that contain a

    processing aid that have an allergenic component, but the label does not declare it.

    Comments and suggestions regarding this document should be submitted to the Dockets

    Management Branch (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061,

    Rockville, MD 20852, Email: fdadockets@oc.fda.gov. Please refer to Docket No. 01D-0316

    when commenting on this document.

    For technical questions concerning food allergens, please contact: Kathy Gombas, Office of Field

    Programs (HFS-615), Center for Food Safety and Applied Nutrition, Food and Drug

    Administration, 200 C St. SW., Washington, DC 20204, 202-205-4231, FAX 202-260-0136.

    For questions concerning regulatory procedures, please contact: Barbara Marcelletti, Office of

    Regional Operations (HFC-130), Office of Regulatory Affairs, Food and Drug Administration,

    5600 Fishers Lane, Rockville, MD 20857, 301-443-6919.

    1

    GUIDANCE ON INSPECTIONS OF FIRMS PRODUCING FOOD

    PRODUCTS SUSCEPTIBLE TO CONTAMINATION WITH

    ALLERGENIC INGREDIENTS

    August 2001 (Editorial Changes Only)

    This guidance is reference material for investigators and other FDA personnel. The

    guidance does not bind FDA and does not confer any rights, privileges, benefits or

    immunities for or on any person(s). An alternative approach may be used if such an

    approach satisfies the applicable statutes, regulations or both.

    INTRODUCTION

    Prior to conducting inspections involving any manufacturer using ingredients that are

    considered allergens, review the general inspectional instructions in the Investigations

    Operations Manual (IOM) Chapter 5 -Establishment Inspections, particularly those in

    IOM 530 -Food Inspections; and review Compliance Program 7321.005 -Domestic

    NLEA, Nutrient Sample Analysis and General Food Labeling Program and Compliance

    Policy Guide Section 555.250, titled “Statement of Policy for Labeling and Preventing

    Cross-contact of Common Food Allergens”.

    Each year the Food & Drug Administration (FDA) receives reports of consumers who

    experienced adverse reactions following exposure to an allergenic substance in foods.

    Food allergies are abnormal responses of the immune system, especially the production

    of allergen-specific IgE antibodies to naturally occurring proteins in certain foods that

    most individuals can eat safely. Frequently such reactions occur because the presence of

    the allergenic substance in the food is not declared on the food label. Current regulations

    require that all added ingredients be declared on the label, yet there are a number of

    issues that have arisen in connection with undeclared allergens that are not clearly

    covered by label regulations. This guidance covers the following problem areas:

    1. Products that contain one or more allergenic ingredients, but the label does not

    declare the ingredient in the ingredient statement;

    2. Products that become contaminated with an allergenic ingredient due to the firm's

    failure to exercise adequate control procedures, e.g. improper rework practices,

    allergen carry-over due to use of common equipment and production sequencing,

    inadequate cleaning;

    3. Products that are contaminated with an allergenic ingredient due to the nature of

    the product or the process; i.e., use of common equipment in chocolate

    manufacturing where interim wet cleaning is not practical and only dry cleaning

    and product flushing is used;

    4. A product containing a flavor ingredient that has an allergenic component, but the

    label of the product only declares the flavor, e.g., natural flavor. Under current

    regulations, firms are not required to declare the individual components of

    2

    flavors, certain colors, and spices. However, firms are encouraged to specifically

    label allergenic components/ingredients that are in spices, flavors, and colors;

    5. Products that contain a processing aid that have an allergenic component, but the

    label does not declare it. Processing aids that contain allergenic ingredients are

    not exempt from ingredient declaration under the incidental additives regulation

    (21 CFR 101.100(a)(3)), and therefore, must be declared.

    FDA believes there is scientific consensus that the following foods can cause serious

    allergic reactions in some individuals and account for more than 90% of all food

    allergies: Peanuts, Soybeans, Milk, Eggs, Fish, Crustacea, Tree nuts, Wheat

    If you are requested to do a follow-up investigation involving an allergic reaction which

    appears to be caused by an undeclared food other than the eight foods listed above, then

    contact the CFSAN / Office of Field Programs regulatory contact listed in the compliance

    program for guidance.

    PRODUCT DEVELOPMENT

    Determine whether the firm identifies potential sources of allergens starting in the

    product development stage. For example, do they identify for each product all

    ingredients, ingredient components, processing aids, rework, processing steps,

    environmental conditions, and product carry over due to use of common equipment? Are

    potential sources of allergen contamination identified at each step?

    Determine whether the products contain allergenic ingredients. For the most frequently

    produced products, request formulas. If formula information is refused, construct

    formulations by observing production.

    Determine if the firm has assessed whether the packaging material used in direct contact

    with the product contains an allergen; e.g., foil coated with wheat ingredient as releasing

    agent.

    Does the firm use processing aids in the manufacture of the food? If so, do the

    processing aids contain allergenic ingredients? If so, what are the allergenic ingredients?

    3

    Does the firm use spices, flavors, or colors that contain allergenic components? If so, do

    these spices, flavors or colors contain allergenic ingredients? If so, what are the

    allergenic ingredients?

    RECEIVING

    Determine whether the firm uses allergenic ingredients.

    Determine how these allergenic ingredients are handled at receiving and how they are

    identified and/or segregated in raw material storage.

    Determine if the firm stores any of these allergenic ingredients in bulk tanks. If yes, how

    are the contents of the bulk tanks identified?

    Determine what the firm’s procedure is for receiving ingredients into the bulk tank and

    what controls are in place to ensure proper product identity at all times.

    Determine if the firm receives any raw materials that are labeled with a statement, such as

    "this product was processed on machinery that was used to process products containing

    (allergen)" or "may contain (allergen)". If so what ingredients? How are such statements

    reflected on the label of the firm’s finished product?

    Determine whether a label from each incoming lot of finished product labels is visually

    checked, either upon receipt or during production, to ensure the ingredient statement is

    correct for the intended product and that it is not a carton of mixed labels.

    EQUIPMENT

    Try to inspect the equipment before processing begins and document the adequacy of

    clean up. For example, is there a build up of residual materials or pockets of residue in

    corners that may contain an allergen from previous runs? What is the condition of the

    conveyor belts? Is there any product build-up above processing zones? Also observe

    whether the firm checks the processing lines for cleanliness prior to production and

    whether


     

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