55 services carry this tag in their source record. Tags come from the provider, not from us — a tag is a claim about what the service does, not proof that it does it well.
Web search built for agents, served over Pocket Network: POST /v1/search with a query and an optional max_results, and get the results back as one JSON object. Results vary run to run, as web search does. GET /v1/version...
Name a drug, food, ingredient, brand or medical device and get one cited FDA recall report: every matching enforcement record across the drug, food and device feeds (firm, class I/II/III, status, reason, distribution, da...
Search US drug products by NDC, brand, generic name, ingredient, manufacturer, dosage form, route, source, or identifier.
FDA recalls and adverse events. Drug, device, and food recall and adverse-event records from openFDA with classification, recalling firm, and reason.
Active recall dashboard for consumer and safety agents. Consolidates CPSC, FDA, USDA FSIS, and NHTSA recalls in one view.
Top trending Polymarket markets by 24h volume — prices, liquidity, volume data
Is this product recalled, product recall check, safety recall lookup, is it safe to use. For shopping and safety agents: takes a product and returns official CPSC recall database rows verbatim plus NHTSA/FDA web scan, wi...
Give it drug names (brand or generic). For each it fuses four openFDA sources - approvals, FAERS adverse events (total, top reactions, serious, deaths), recalls and the boxed warning - into ONE composed safety brief. Key...
Cheapest endpoint: liveness plus x402 payment pipeline check — Returns ok with the server time and whether this call was paid. Use it to verify your x402 client end to end before spending on data endpoints.
Search FDA 510(k) premarket clearances (openFDA) by applicant, three-letter product code, K number or device name: decision and date, clearance type, device class, regulation number, the FDA classification name, medical...
FDA inspection history for a manufacturer from public FDA records. Give an FDA FEI number or firm name and get the inspection classifications (Official, Voluntary or No Action Indicated) with the trend, plus the Form-483...
Search FDA medical-device recall / enforcement records (openFDA): recalling firm, classification (Class I/II/III), reason, distribution, and dates. Live FDA data, no key.
Search FDA drug recall / enforcement records (openFDA): recalling firm, classification (Class I/II/III), reason, distribution, and dates. Live FDA data, no key.
Search FDA food recall / enforcement records (openFDA): recalling firm, classification, reason (allergen, contamination, etc.), distribution, and dates. Live FDA data, no key.
FDA PDUFA Calendar ($0.04): upcoming FDA target-action dates as disclosed by sponsors in their own SEC EDGAR filings (10-K/10-Q/8-K) — not an estimate from trial-phase metadata. Body { ticker?, upcoming_days?: 1..730, in...
FDA drug label lookup — the newest prescribing information for a brand or generic drug name: boxed warning, indications, dosage, contraindications, warnings, adverse reactions and drug interactions as previews or one sec...
Summarize FDA medical device adverse event reports (openFDA MAUDE) for a device name, brand, product code or manufacturer: total matching reports, counts by event type (death, injury, malfunction), the most reported devi...
FDA drug labeling (openFDA SPL) by brand or generic name, or by NDC: boxed warning, indications and usage, dosage and administration, contraindications, and warnings and precautions, with manufacturer, routes, applicatio...
Look up the FDA National Drug Code directory (openFDA) by NDC or by brand or generic name: product NDC, labeler, dosage form, routes, active ingredients with strengths, marketing category and application number, pharmaco...
FDA drug recall lookup — enforcement reports naming a drug, newest first, with recall class and its meaning, status, reason, product description, recalling firm, dates, distribution and quantity. Use to check whether a d...
Returns US FDA recalls (enforcement reports) for food, drugs or medical devices, filtered by firm, product text, class (I, II, III), US state, status and report date range.
21 CFR 101.9 Nutrition Facts panel format and added-sugars %DV check.
DSHEA structure/function claim, 30-day notification and FDA disclaimer check.
Classify device pathway: Class I exempt, Class II 510(k), or general wellness.