{"uid":"cap_VyK9IKEUObxEK-1Txnfkx","slug":"arakel-fda-device-recalls-lookup-bac12254","name":"ARAKEL FDA Device Recalls Lookup","description":"Machine-verifiable official-source evidence with free preflight and x402 USDC payments on Base.","url":"https://proof.arakelproof.space/v1/fda-device-recalls","method":"GET","headers":{},"bodySchema":{"type":"object","$schema":"https://json-schema.org/draft/2020-12/schema","required":["input"],"properties":{"input":{"type":"object","required":["type","method"],"properties":{"type":{"type":"string","const":"http"},"method":{"enum":["GET"],"type":"string"},"queryParams":{"type":"object","required":["q"],"properties":{"q":{"type":"string","description":"FDA medical device recall lookup by device, brand, firm, recall number, or product term using official openFDA enforcement data."},"to":{"type":"string","format":"date-time","description":"Optional UTC end. Defaults to now."},"from":{"type":"string","format":"date-time","description":"Optional UTC start. Defaults to the last 365 days."}}}},"additionalProperties":false},"output":{"type":"object","required":["type"],"properties":{"type":{"type":"string"},"example":{"type":"object"}}}}},"responseSchema":{"type":"json","example":{"result":"OBSERVED|NOT_OBSERVED|INCONCLUSIVE","schema":"arakel.machine-evidence.v2","source":{"id":"fda"},"evidence":[{}],"signature":{"alg":"Ed25519"},"observed_count":1}},"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.005","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"registry","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":"$0.005/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.005","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.005","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_ZQpK_7is1FNSOQ04ggDLQ","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.005","costPer":"request","priority":0,"asset":null,"unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Checks whether a specific medical device or manufacturer appears in FDA device recall records and returns a signed machine-evidence proof of OBSERVED, NOT_OBSERVED, or INCONCLUSIVE status.","exampleAgentPrompt":"Can you check the FDA device recall database and give me a signed machine-evidence proof of whether the Medtronic MiniMed 670G insulin pump has any active recalls on record?","exampleUseCases":[{"title":"Pre-procurement device safety check","prompt":"Before we finalize this purchase order, can you verify in the FDA recall database whether the Stryker Triathlon knee implant system has any recall history and give me a signed proof I can attach to the audit file?"},{"title":"Supplier due diligence for medical distributor","prompt":"I'm vetting a new supplier — can you pull FDA device recall records for all devices manufactured by Zimmer Biomet and tell me if any are flagged as recalled, with a signed evidence report?"},{"title":"Regulatory compliance attestation","prompt":"Our compliance team needs a machine-signed NOT_OBSERVED proof from the FDA device recall database for the Philips Respironics DreamStation CPAP — can you get that and confirm it shows no recalls?"}],"resultDescription":"A signed JSON response containing a result field (OBSERVED, NOT_OBSERVED, or INCONCLUSIVE), an array of evidence records from the FDA recall database, the source identifier ('fda'), an observed count, and an Ed25519 cryptographic signature — conforming to the arakel.machine-evidence.v2 schema. The signature allows downstream systems to verify the proof was generated by ARAKEL without re-querying the source.","failureModes":["Device or manufacturer not found in FDA database — returns NOT_OBSERVED with zero evidence records","Ambiguous query matches multiple devices — may return INCONCLUSIVE status","FDA source temporarily unavailable — may return INCONCLUSIVE or error","Invalid or missing query parameters — returns 4xx with error description","Payment not completed — request blocked before reaching source","Rate limiting or quota exceeded — returns 429 or payment-required response"],"whenToPreferThis":"Choose this endpoint when you need a cryptographically signed, machine-verifiable proof of FDA device recall status — not just a raw database query result. It is especially valuable in compliance workflows, supplier audits, or automated procurement pipelines where a tamper-evident, source-attributed evidence record is required. Prefer this over direct FDA database queries when your workflow needs the NOT_OBSERVED proof pattern (proving absence of recall) or when integrating with systems that validate Ed25519-signed evidence. At $0.005 per call it is cost-effective for high-frequency automated checks.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-14T06:41:09.366Z","isFirstParty":false}