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FDA Drug Recall Enforcement Quarterly Archive

Immutable normalized edition of current-quarter FDA drug recall enforcement reports with classification, firm, product, reason, distribution, and first-party evidence fields.

What this product does

Immutable normalized edition of current-quarter FDA drug recall enforcement reports with classification, firm, product, reason, distribution, and first-party evidence fields.

Who it is for

Not published yet.

Problems solved

Not published yet.

Update cadence

4 hours ago

Pricing and access note

Not published yet. Pricing will appear on the verified external marketplace listing.

Source and provenance note

Foundry product package: ProductStudio public-safe metadata

Limitations

Review the sample, schema, source notes, marketplace availability, and cadence before depending on this product in production.

Delivery options

Not published yet. A link appears only after a verified external marketplace destination exists.

Sample and schema preview

  • recall_number (string)
  • report_date (string)
  • recall_initiation_date (string)
  • classification (string)
  • status (string)
  • recalling_firm (string)
  • product_description (string)
  • reason_for_recall (string)
  • product_quantity (string)
  • distribution_pattern (string)
{
  "rows": [
    {
      "state": "CA",
      "status": "Ongoing",
      "country": "United States",
      "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number.exact%3A%22D-0612-2026%22&limit=1",
      "report_date": 20260701,
      "recall_number": "D-0612-2026",
      "classification": "Class II",
      "recalling_firm": "Amgen, Inc.",
      "product_quantity": "934577 bottles",
      "reason_for_recall": "Presence of Foreign Substance.",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "product_description": "Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.",
      "distribution_pattern": "Nationwide within the United States",
      "recall_initiation_date": 20260604
    },
    {
      "state": "CA",
      "status": "Ongoing",
      "country": "United States",
      "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number.exact%3A%22D-0615-2026%22&limit=1",
      "report_date": 20260701,
      "recall_number": "D-0615-2026",
      "classification": "Class II",
      "recalli

Related products and use cases

Related products and use-case links are not published yet.