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FDA Recalls and Enforcement Actions
x402
FDA Recalls and Enforcement Actions is a paid API for AI agents from x402-filings.datalayer.workers.dev, paid per call via x402, $0.01/call, status unknown (last checked 2026-10-12).
Queries FDA recall and enforcement records across drugs, devices, and food, normalized into a unified schema with classification, reason, distribution scope, and recalling firm.
Price / call$0.01
Success—
StatusUnknown
How this service works
FDA recall and enforcement records across drug, device and food, normalised into one shape with classification, reason, distribution scope and firm. Queryable by firm, product, classification and date. One product type returning nothing never fails the call — the three openFDA endpoints are independent and a gap in one is not a gap in the others.
Output
Returns a list of normalized FDA recall records (up to 100 per call) drawn from the drug, device, and food openFDA endpoints, each record including: recalling firm name, product description, recall classification (Class I/II/III), reason for recall, distribution scope, and report date. Results from all three product-type endpoints are merged into a single unified shape; if one product type returns no results it does not cause the call to fail.
Example use cases
Pharma counterparty risk screening
“Before we finalize this supplier agreement, can you check if NovaBay Pharmaceuticals has any recent FDA enforcement actions or recalls — especially Class I drug recalls in the last 12 months?”
Food safety contamination alert
“I need a list of all FDA food recalls related to contamination or allergens filed since January 2025, up to 50 results, so I can flag any that match our distribution partners.”
Medical device regulatory due diligence
“Pull all Class II and Class I device recalls from the past two years and filter for any mentions of 'sterilization' in the recall reason — we're evaluating a device manufacturer acquisition.”
Technical details
Endpoint
GEThttps://x402-filings.datalayer.workers.dev/v1/fda/enforcement?utm_source=zero.xyzWhen to prefer
Choose this endpoint when you need a unified, normalized view of FDA enforcement across drug, device, and food categories without having to query three separate openFDA endpoints and reconcile schemas yourself. It is especially well-suited for compliance screening, counterparty due diligence, supply chain risk monitoring, and regulatory research workflows. Prefer it over raw openFDA queries when you need cross-product-type aggregation in a single call, or when you want to filter by firm name, recall classification, and date range simultaneously.
Side effects
- No records found for the specified firm, date range, or classification — returns empty result set rather than an error
- Invalid product type value (not drug/device/food/all) may return an error or empty result
- Date range malformed (non-ISO format) may cause a query failure
- Upstream openFDA API outage for one product category returns partial results for the remaining categories
- Rate limiting or payment failure (x402) may block the request
- Overly broad queries may hit the 100-record limit and truncate results
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Tags
x402
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