{"uid":"cap_02oGldqvdERjXv7tV8LWO","slug":"fda-recall-watch-063e2205","name":"FDA Recall Watch","description":"FDA recall and enforcement search across drugs, food/cosmetics, and medical devices (85,000+ actions). Returns classification (Class I/II/III), recall reason, product description, status, and distribution pattern. Seam cap: fills the product-safety layer missing from drug-intel + company-due-diligence chains. No API key required.","url":"https://the-stall.intuitek.ai/cap/fda-recall-watch","method":"GET","headers":{},"bodySchema":{"type":"object","properties":{"required":{"type":"string"},"properties":{"type":"string"}}},"responseSchema":null,"example":{"request":{"input":{"type":"http","method":"GET","queryParams":{"limit":5,"query":"acetaminophen","class_filter":"any","product_type":"drugs"}}},"response":{"query":"acetaminophen","totals":{"drugs":260},"recalls":[{"status":"Ongoing","event_id":"98136","severity":2,"brand_names":["OXYCODONE AND ACETAMINOPHEN"],"recall_date":"2025-12-16","product_type":"Drugs","generic_names":["OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN"],"recall_number":"D-0254-2026","classification":"Class II","recalling_firm":"SpecGx, LLC","termination_date":null,"reason_for_recall":"Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.","voluntary_mandated":"Voluntary: Firm initiated","product_description":"Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01.","distribution_pattern":"Nationwide"},{"status":"Ongoing","event_id":"98136","severity":2,"brand_names":["OXYCODONE AND ACETAMINOPHEN"],"recall_date":"2025-12-16","product_type":"Drugs","generic_names":["OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN"],"recall_number":"D-0255-2026","classification":"Class II","recalling_firm":"SpecGx, LLC","termination_date":null,"reason_for_recall":"Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.","voluntary_mandated":"Voluntary: Firm initiated","product_description":"Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01.  Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493","distribution_pattern":"Nationwide"},{"status":"Ongoing","event_id":"97850","severity":2,"brand_names":["TYLENOL EXTRA STRENGTH"],"recall_date":"2025-10-21","product_type":"Drugs","generic_names":["ACETAMINOPHEN"],"recall_number":"D-0121-2026","classification":"Class II","recalling_firm":"Kenvue Brands LLC","termination_date":null,"reason_for_recall":"Defective Container","voluntary_mandated":"Voluntary: Firm initiated","product_description":"TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04.","distribution_pattern":"U.S. Nationwide - CO, IL, OH and IN."},{"status":"Ongoing","event_id":"97809","severity":2,"brand_names":["AEROTAB PAIN RELIEVER"],"recall_date":"2025-10-17","product_type":"Drugs","generic_names":["PAIN RELIEVER"],"recall_number":"D-0155-2026","classification":"Class II","recalling_firm":"Aero Healthcare","termination_date":null,"reason_for_recall":"Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine 65mg. The inner pouch correctly states the ingredients are Aspirin (NSAID)*500mg and Caffeine 32.5mg.","voluntary_mandated":"Voluntary: Firm initiated","product_description":"Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further packaged in a 50-count box, AERO TAB, Manufactured for AERO HEALTHCARE US, Valley-Cottage, NY, 10989, NDC 55305-135-01","distribution_pattern":"US Nationwide."},{"status":"Ongoing","event_id":"97453","severity":2,"brand_names":["ACETAMINOPHEN"],"recall_date":"2025-08-20","product_type":"Drugs","generic_names":["ACETAMINOPHEN"],"recall_number":"D-0596-2025","classification":"Class II","recalling_firm":"Baxter Healthcare Corporation","termination_date":null,"reason_for_recall":"Discoloration","voluntary_mandated":"Voluntary: Firm initiated","product_description":"Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60.","distribution_pattern":"U.S.A. Nationwide"}],"class_filter":"any","generated_at":"2026-06-12T05:11:20.273Z","product_type":"drugs"}},"exampleRequest":{"limit":5,"query":"acetaminophen","class_filter":"any","product_type":"drugs"},"tags":["x402"],"displayCostAmount":"0.034","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"settled","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":"$0.034/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.034","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.034","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_t5p4wCld0Z62waN5mwOAZ","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.034","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Searches FDA recall records across drugs, food, and medical devices by keyword, company, ingredient, or recall classification","exampleAgentPrompt":"Search the FDA recall database for any Class I recalls involving Listeria in food products — show me up to 5 results.","exampleUseCases":null,"resultDescription":"Returns a list of FDA recall records (up to the requested limit per category) including recalled product names, companies, recall classification (Class I/II/III), reason for recall, and relevant identifiers, fetched in parallel across drugs, food, and/or devices depending on the product_type filter.","failureModes":["No recalls found for the given query — empty result set returned","Invalid product_type or class_filter enum value causes a 400-level error","FDA API upstream unavailability causes a timeout or 5xx error","Query too broad returns maximum results without covering all matches","limit parameter outside 1–10 range rejected with validation error"],"whenToPreferThis":"Use this endpoint when an agent needs to check FDA recall status for any drug, food product, or medical device — especially for safety research, compliance checks, or consumer alerts. Ideal when the search spans multiple product categories simultaneously. Prefer over manual FDA website searches or generic web search when structured recall data with classification filtering is needed.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-13T12:57:56.294Z","isFirstParty":false}