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    Solution · Food

    Food traceability software built on the substance, not the pallet.

    Most traceability tools trace boxes. Regulators, retailers and recalls care about what is inside the box. Worldover holds ingredients, lots, formulas and shipments as live objects, so a Critical Tracking Event is recorded once and the Key Data Elements regenerate wherever they are demanded: an FDA request, a retailer audit, a recall at 9pm on a Friday.

    Quick answer

    Food traceability software records the movement and transformation of food and food ingredients at lot level, so that any product can be traced one step back and one step forward. Under FSMA 204 in the US, firms handling Food Traceability List items must capture Key Data Elements (KDEs) at defined Critical Tracking Events (CTEs) and produce a sortable electronic record within 24 hours of an FDA request. Worldover captures those events inside normal operations, holds them against the live lot record, and generates the sortable spreadsheet on demand rather than assembling it under pressure.

    • FSMA 204 Key Data Elements captured at every Critical Tracking Event
    • Lot-level genealogy from raw material to shipped case
    • Sortable electronic record produced within 24 hours
    • One step back, one step forward in a single query
    • Recall simulation before you need the real one
    • Shared substance master with supplements, cosmetics and chemicals

    How this connects to Worldover

    Replacing five subscriptions with one system you actually run the business on?

    Worldover is the AI operating system for chemicals, cosmetics and supplement businesses. One platform, one data model, custom-built around each team.

    See how Worldover works

    Why traceability projects usually fail

    Traceability is rarely a data-capture problem. Most manufacturers already record lot numbers somewhere. The failure is that the records live in different systems that never agreed on what a lot is: goods-in records a supplier lot, production records a batch, the WMS records a pallet, and the customer service inbox records a complaint against a case code. Linking them is a manual reconstruction exercise, done once a year for the mock recall and then forgotten.

    That reconstruction is what breaks the 24-hour clock. When the FDA asks for a sortable record, you are not being asked to find the data, you are being asked to have already joined it.

    Critical Tracking Events, and what Worldover captures at each

    Critical Tracking EventKey Data Elements held
    Harvesting / first receivingTraceability lot code, location description, commodity, variety, quantity, date, reference document.
    ReceivingLot code, immediate previous source, receipt date and location, quantity, reference document.
    TransformationInput lot codes and quantities, new lot code assigned, output quantity, date, location. This is the step generic WMS tools cannot do.
    CreatingNew traceability lot code, product description, quantity, date, creating location.
    ShippingLot code, immediate subsequent recipient, ship date and location, quantity, reference document.

    The transformation problem

    Transformation is where most traceability stacks quietly break. A blend of nine input lots produces one output lot, and the link between them either exists as a formula-level genealogy record or it does not exist at all. Worldover builds that link automatically because the formula, the batch and the inventory movement are the same object. Ask which finished lots contain supplier lot 4417 and the answer is a query, not an investigation.

    Worldover for this

    Traceability that is a by-product of operations

    Stop running a separate traceability project. Capture the events where the work happens and generate the record when someone asks.

    See how Worldover works

    Recall response, simulated before it matters

    • Trace back from a finished lot to every input lot and supplier, in one step.
    • Trace forward from a suspect supplier lot to every finished lot, customer and shipment it reached.
    • Scope the exposure in units, value and customers before you decide what to withdraw.
    • Generate the sortable record in the format the FDA asks for, with the audit trail of who produced it.
    • Run it as a drill on any lot, any time, without pulling the team off production.

    Willow AI in the workflow

    Willow answers traceability questions in plain language: which customers received product containing this supplier lot, which lots are still in stock, what the total exposure is. It drafts the customer notification and the internal timeline from the live records, and flags gaps in KDE capture before an auditor finds them.

    Who this fits

    Specialty food and ingredient manufacturers, flavour and fragrance houses, nutraceutical and functional food producers, and contract manufacturers running mixed food and non-food portfolios. If you already run cosmetics or chemicals lines, the same substance master covers all of them. See nutraceutical ERP and HACCP software.

    FAQs

    Common questions.

    See Worldover on your operation.

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