datasets / product
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",
"recalliRelated products and use cases
Related products and use-case links are not published yet.