How to verify container separation for allergen control

Assign containers by risk assessment; check cleaning effectiveness with records and verification.

15 June 2025Updated 23 September 2026

Short answer

Identify allergen-containing products and contact/spread pathways in the site risk assessment. Base container allocation, labels, loading sequence and cleaning method on that assessment; do not assume every allergen needs its own container. Record cleaning verification method and results against container ID. If labels or cleaning evidence are missing, segregate the unit and consult quality; decide next use under the approved procedure.

Allergen separation should follow the site risk assessment for products and contact pathways; one container-allocation rule does not fit every operation.

Identify transfer pathways. Map products, spill/leak potential, powder spread, contact surfaces and the next load. Define in the quality plan which flows can be controlled by cleaning and which require dedicated equipment, with rationale.

Link container ID, allergen group or use status, visible label, cleaning date and verification result in one record. If colour coding is used, support it with a number or written code.

Check the container and marking before loading; do not release it for use if cleaning evidence is missing. For a discrepancy, segregate the next load and record corrective action and quality approval.

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Topics:Regulations and standards Containers and equipment

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