{
  "status": "pass",
  "version": "2026-09-01-v1",
  "capturedAt": "2026-09-01T09:59:31Z",
  "grain": {
    "keywordResult": "one openFDA food-enforcement report row per unique recall_number",
    "publicDataset": "one manually reviewed event_id per explicit supplement or functional-nutrition event"
  },
  "counts": {
    "apiReportedRows": 25,
    "downloadedUniqueRecallNumbers": 25,
    "keywordMatchedDistinctEvents": 10,
    "includedSupplementReportRows": 9,
    "includedSupplementDistinctEvents": 6,
    "adjacentPsychoactiveReportRowsExcluded": 11,
    "conventionalCandyOrBeverageReportRowsExcluded": 5
  },
  "checks": {
    "apiTotalMatchesDownloadedRows": true,
    "recallNumberIsUnique": true,
    "everyReturnedEventWasManuallyClassified": true,
    "publicDatasetHasOneRowPerIncludedEvent": true,
    "publicDatasetHasSixUniqueEventIds": true,
    "noMarketRateOrIncidenceClaimIsSupported": true
  },
  "limitations": [
    "Keyword matching can miss a relevant record whose product description contains no token beginning with gumm.",
    "The snapshot has no denominator for products manufactured or sold and cannot establish a gummy-industry recall rate.",
    "Multiple recall_number rows can belong to one event_id, so report-row counts are not independent event counts.",
    "Supplement relevance and buyer-readable reason categories are Sucotond USA analytical labels, not FDA classifications.",
    "openFDA records can be corrected, updated, completed or terminated after capture."
  ]
}