{"uid":"cap_v-qtcnnwAiTMSRLx3mL0F","slug":"fda-approval-recall-feed-0440a9a3","name":"FDA Approval & Recall Feed","description":"Pay-per-call data & tool APIs","url":"https://api.timzinin.com/api/fda-approval-feed","method":"POST","headers":{},"bodySchema":{"type":"object","properties":{"limit":{"type":"integer","maximum":50,"minimum":1},"dataset":{"enum":["approvals","recalls","both"],"type":"string"},"queries":{"type":"array","maxItems":25},"maxConcurrency":{"type":"integer","maximum":8,"minimum":1}}},"responseSchema":{"type":"json","example":{"meta":{"run_ms":1200,"settled":true,"item_count":1},"results":[{"firm":"Infusion Options, Inc.","type":"recall","found":true,"reason":"Lack of Assurance of Sterility","status":"Terminated","product":"PEMBROLIZUMAB 200 MG / 100 ML NS IVPB, Rx Only, Infusion Options, Inc. 5924 13the Ave, Brooklyn, NY 11219-4934, 718-283-7233","summary":"Infusion Options, Inc. recall (Class II) — PEMBROLIZUMAB 200 MG / 100 ML NS IVPB, Rx Only, Infusion Options, Inc. 5924 13the Ave, Brooklyn, NY 11219-4934, 718-283-7233 — Lack of Assurance of Sterility.","checkedAt":"2026-07-26T13:58:04.917Z","reportDate":"2019-08-21","sourceQuery":"pembrolizumab","classification":"Class II"}]}},"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.02","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"probe","requiresHandshake":false,"reviewCount":0,"rating":{"score":"0.00","successRate":"0.00","reviews":0,"stars":null,"state":"unrated"},"availabilityStatus":"unknown","priceObserved":null,"sessionDeposit":null,"pricing":{"kind":"static","summary":"$0.02/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.02","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.02","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_Q1oA4S60L9hH_b6uzGcD6","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.02","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Looks up FDA drug approval and recall records for a given drug or product name, returning classification, status, reason, and summary details","exampleAgentPrompt":"Can you check the FDA recall and approval feed for pembrolizumab and tell me if there are any active or terminated recalls, including the classification and reason?","exampleUseCases":[{"title":"Drug safety check before dispensing","prompt":"Before we dispense this batch of pembrolizumab, can you check the FDA recall feed to see if there are any recalls on it and what class they are?"},{"title":"Pharmaceutical compliance audit","prompt":"Run an FDA recall lookup on all the compounded infusion products from Infusion Options Inc. and summarize any Class II recalls with their reasons and current status."},{"title":"Patient medication safety verification","prompt":"My patient was prescribed methotrexate — can you check the FDA database to see if there are any outstanding recalls or safety issues with it, and give me the recall reason and classification if there are?"}],"resultDescription":"Returns a JSON object with a meta block (run time in ms, settlement status, item count) and a results array. Each result includes the firm name, recall type, found flag, reason for recall, current status (e.g. Terminated), full product description, a plain-language summary, the date checked, the original report date, the source query used, and the FDA recall classification (e.g. Class I, Class II, Class III).","failureModes":["Drug or product name not found in FDA database returns empty results array with item_count 0","Misspelled or ambiguous drug names may return no matches or unrelated records","FDA data latency may mean very recent recalls are not yet reflected","Payment failure via x402 protocol results in 402 response before query is processed","Network timeout if FDA upstream is slow, reflected in elevated run_ms"],"whenToPreferThis":"Use this endpoint when you need structured, per-call FDA recall and approval data for specific drugs or pharmaceutical products without maintaining a full FDA dataset subscription. It is ideal for compliance checks, patient safety workflows, or enriching drug records in real time. Prefer this over raw FDA API access when you want a normalized, pre-parsed JSON response with classification and status fields already extracted.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-15T06:42:09.354Z","isFirstParty":false}