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Allergen Control Program Overview

The document outlines an allergen control program with five stages: receiving, storage, documentation, production, and labeling. It provides detailed procedures for each stage to ensure allergenic ingredients are properly managed and do not contaminate non-allergenic products.

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100% found this document useful (1 vote)
14 views2 pages

Allergen Control Program Overview

The document outlines an allergen control program with five stages: receiving, storage, documentation, production, and labeling. It provides detailed procedures for each stage to ensure allergenic ingredients are properly managed and do not contaminate non-allergenic products.

Uploaded by

Johnny
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd

Insert Letterhead

Date Created   Revision   Approval  

Title Allergen Control Program

Objective: to ensure that allergenic ingredients do not find their way into products for they are not
intended.
There are five stages where allergens need to be managed, these are:
1. Receiving
2. Storage
3. Documentation
4. Production
5. Labeling

Receiving
1. Containers/super sacks/bags/other must have legible labels clearly indicating their contents. Any
packaging that lacks legible labels are to be rejected.
2. Damaged containers/super sacks/bags/other are to be rejected.
3. Trucks are inspected for cleanliness prior to accepting material. If it is determined that
contamination has occurred, the load is to be rejected.
4. In all instances, use the “Rejected material” form.

Storage
1. Spills are to be cleaned as soon as possible to minimize cross-contamination.
2. Storage containers are to be kept clean and sealed. Tape bags closed, “four fold” boxes, replace
lids.
3. Whenever possible, separate storage areas are to be maintained for allergen/non-allergen.
4. Labels are clear, legible, and easy to understand. Replace labels if they fail inspection.

Documentation
1. Suppliers are subject to evaluation prior to approval.
2. They must provide specifications.
3. They should have COA/Letters of Guarantee available.
4. They must be able to provide internal allergen control program for review.

Production
1. Whenever possible, schedule non-allergens first.
2. Run “like with like”
3. If not possible to run non-allergens first, add allergens in a fashion that does not contaminate
equipment.
4. Rework is by plant management approval only.
5. Double check all ingredients prior to opening/handling.
6. Clean area after allergens are introduced.
7. Re-seal and store correctly any partial containers that may be allergenic.
8. Discard gloves and other PPE that have come in contact with allergens.
9. Thoroughly cleanse tools/utensils/containers that come in contact with allergens.

Labeling
1. Quality tech is notified when a new blend is to be produced. Quality will review ingredients and
determine what changes to are required for labeling.
2. Plant management issues approval for labeling.
3. Supervisors/Operators are trained to recognize new labels and instructed when to change over
during production.

Common questions

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To minimize allergen cross-contamination in a food production facility, recommended storage practices include immediate cleaning of spills to prevent their spread, maintaining clean and sealed storage containers, and taping bags closed securely. Boxes should be properly folded, and lids replaced after use. Additionally, maintaining separate storage areas for allergenic and non-allergenic products, when possible, further reduces the likelihood of cross-contamination. Labels on containers must be clear, legible, and easy to understand, and replaced if damaged or lacking clarity .

Plant management plays a crucial role in ensuring effective implementation of an allergen control program by providing oversight and authorization in multiple areas. This includes issuing approval for rework procedures and new labeling prior to production, as well as handling training programs for supervisors and operators regarding allergen management. They are instrumental in policy enforcement and facilitating communication among departments to maintain high standards of allergen safety throughout the production process .

The staging of allergen management enhances the safety and quality of food products by addressing allergen control at multiple levels: receiving, storage, documentation, production, and labeling. Legible labels and inspection of containers prevent contaminated raw materials from entering the supply chain. Strict cleaning protocols in storage reduce the risk of allergen cross-contamination. Supplier documentation ensures only approved sources are used. During production, scheduling and procedural steps limit equipment contamination. Labeling ensures accurate consumer information about allergens in products. Together, these stages form a comprehensive system that reduces the risk of allergen mishaps and promotes product safety .

Cross-functional collaboration within a production facility enhances allergen control efforts by leveraging diverse expertise across departments to create a cohesive strategy. For instance, quality control can work with production to ensure ingredient integrity, while storage teams coordinate with procurement to manage supply chain risks. Collaboration fosters comprehensive training protocols, allowing supervisors and operators to effectively implement allergen detection and management practices. Moreover, ongoing communication ensures accurate labeling, enhances incident response, and allows for continuous improvements in allergen management processes .

Critical steps in the production process to handle allergenic materials safely include scheduling non-allergenic materials first, processing like products together ("like with like"), ensuring allergenic materials are added in a contamination-controlled manner, and double-checking ingredients before handling. It is essential to clean the production area thoroughly after allergens are processed, discard contaminated personal protective equipment (PPE), and cleanse all tools in contact with allergens. Proper resealing and storage of leftover allergenic materials are also crucial, safeguarding against contamination and maintaining product integrity .

During the labeling stage of allergen management, several procedures ensure compliance with protocols. Firstly, quality technicians are notified when a new blend is produced, prompting a review of ingredients to determine necessary labeling changes. Plant management approves these labels, ensuring they are consistent with the allergenic content of the product. Additionally, supervisors and operators receive training to recognize new labels and are instructed on when to switch labels during production to prevent mislabeling and ensure consumer safety .

To prevent cross-contamination between allergenic and non-allergenic products in a production facility, several mechanisms are implemented. Non-allergenic products are scheduled first whenever feasible to minimize contamination risk. Similar products are processed consecutively to reduce equipment contamination. If allergens must be included first, they are added in a way that does not contaminate the equipment. After processing allergens, the production area is thoroughly cleaned, gloves and other PPE that have contacted allergens are discarded, and tools, utensils, and containers that made contact with allergens are cleansed thoroughly. Additionally, all ingredients are double-checked before being opened or handled .

Failure to properly document supplier allergen control programs poses significant risks to food production operations as it can lead to the use of raw materials with undisclosed allergens, thereby increasing the risk of cross-contamination. Without certificates such as COA or Letters of Guarantee and documentation of the supplier's internal allergen control measures, the trustworthiness and compliance of suppliers cannot be fully verified. This lack of documentation undermines traceability efforts, potentially exposes the company to legal liabilities, and endangers consumer health if allergens are unintentionally introduced into products .

Inspecting transportation vehicles during the receiving stage of allergen management is essential because it ensures they have not previously transported allergenic materials without adequate cleaning, thereby reducing the risk of contamination. Vehicles are inspected for cleanliness, and any that pose a contamination risk have their loads rejected. This step helps to secure the integrity of non-allergenic raw materials before they enter the production facility, preventing unintentional allergen introduction .

Documentation is crucial in an allergen control program because it ensures traceability and compliance with safety standards. Suppliers must undergo evaluation prior to approval and provide detailed specifications, as well as Certificates of Analysis (COA) or Letters of Guarantee, demonstrating their internal allergen control measures. This documentation allows the facility to verify that all measures are in place to prevent allergen cross-contamination and ensures the documented processes are followed consistently during audits and inspections .

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