2s.io FDA Drug Recall Enforcement Reports is a paid API for AI agents from 2s.io, paid per call via x402, $0.0024/call, status unknown (last checked 2026-09-14).
Fetches FDA drug recall enforcement reports from OpenFDA, filterable by drug name, recall status, and classification, sorted newest first.
FDA drug recall enforcement reports, newest first. All filters optional. Each record includes recall number, status (Ongoing/Completed/Terminated/Pending), classification (Class I/II/III), product description, reason for recall, initial-notification mechanism, voluntary-vs-mandated flag, recalling firm name + city/state/country, distribution pattern, and recall + report dates. Backed by OpenFDA's /drug/enforcement endpoint; data is public-domain US government records.
A list of up to 100 FDA drug recall records sorted newest first, each containing recall number, status (Ongoing/Completed/Terminated/Pending), classification (Class I/II/III), product description, reason for recall, initial notification mechanism, voluntary-vs-mandated flag, recalling firm name with city/state/country, distribution pattern, and recall and report dates.
GEThttps://2s.io/api/gov/fda-recallsUse this endpoint when you need US FDA drug recall enforcement data sourced directly from OpenFDA, especially when you need to filter by drug name, recall status, or severity classification. Prefer this over scraping FDA.gov directly or building your own OpenFDA integration, as it provides a clean, structured, paid API with consistent schema.
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{
"city": "Woburn",
"state": "MA",
"status": "Ongoing",
"country": "United States",
"reportDate": "2024-11-27",
"productType": "Drugs",
"recallNumber": "D-0058-2025",
"recallingFirm": "Safecor Health, LLC",
"classification": "Class II",
"reasonForRecall": "cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01",
"distributionPattern": "USA nationwide.",
"initialNotification": "Letter",
"recallInitiationDate": "2024-11-11"
},
{
"city": "East Windsor",
"state": "NJ",
"status": "Ongoing",
"country": "United States",
"reportDate": "2024-08-28",
"productType": "Drugs",
"recallNumber": "D-0641-2024",
"recallingFirm": "Aurobindo Pharma USA Inc",
"classification": "Class I",
"reasonForRecall": "Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles, Distributed by: Aurohealth LLC, 279 Princeton-Hightstown Road, East Windsor, NJ , Made in India, NDC 58602-882-21.",
"distributionPattern": "NJ, NY & PA",
"initialNotification": "Letter",
"recallInitiationDate": "2024-07-11"
},
{
"city": "Dublin",
"state": "OH",
"status": "Terminated",
"country": "United States",
"reportDate": "2024-01-03",
"productType": "Drugs",
"recallNumber": "D-0170-2024",
"recallingFirm": "CARDINAL HEALTHCARE",
"classification": "Class II",
"reasonForRecall": "CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Low Dose ASPIRIN, 81 mg, 120 Enteric Coated Tablets, Distributed by: Rugby Lavoratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1234-41",
"distributionPattern": "Nationwide USA",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-26"
},
{
"city": "Chesapeake",
"state": "VA",
"status": "Ongoing",
"country": "United States",
"reportDate": "2022-08-31",
"productType": "Drugs",
"recallNumber": "D-1424-2022",
"recallingFirm": "Family Dollar Stores, Llc.",
"classification": "Class II",
"reasonForRecall": "CGMP Deviations: product held outside appropriate storage temperature conditions.",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "FW ASPIRIN CHEWABLE TABLET 36CT SKU 913990 GS ENTERIC ASPIRIN TABLET 120 CT SKU 913724 BAYER BACK BODY EX STRGTH CAPLETS 24CT SKU 900438 BAYER LOW DOSE 81 MG TABLET 120 CT SKU 916070 BAYER ASPIRIN 325MG TABLET 24CT SKU 913996 BAYER LOW DOSE TABLET 32CT SKU 915641 BAYER 81MG CHEWABLE TABLET 36 CT SKU 916078 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.",
"distributionPattern": "Nationwide within the United States",
"initialNotification": "Other",
"recallInitiationDate": "2022-06-23"
},
{
"city": "Mahwah",
"state": "NJ",
"status": "Ongoing",
"country": "United States",
"reportDate": "2022-07-27",
"productType": "Drugs",
"recallNumber": "D-1282-2022",
"recallingFirm": "Glenmark Pharmaceuticals Inc., USA",
"classification": "Class III",
"reasonForRecall": "Failed Tablet/Capsule Specification : Capsule breakage",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-405-60.",
"distributionPattern": "USA Nationwide",
"initialNotification": "Letter",
"recallInitiationDate": "2022-06-29"
},
{
"city": "Highland",
"state": "NY",
"status": "Terminated",
"country": "United States",
"reportDate": "2022-02-16",
"productType": "Drugs",
"recallNumber": "D-0538-2022",
"recallingFirm": "ULTRAtab Laboratories, Inc.",
"classification": "Class II",
"reasonForRecall": "CGMP Deviations",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "HPC Tablet (Acetaminophen 110 mg, Aspirin 162 mg, Caffeine 32.4 mg, Salicylamide 152 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62969-242-00",
"distributionPattern": "Bulk product was distributed to 3 distributors who may have distributed finished product.",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-26"
},
{
"city": "New Paltz",
"state": "NY",
"status": "Terminated",
"country": "United States",
"reportDate": "2022-02-09",
"productType": "Drugs",
"recallNumber": "D-0467-2022",
"recallingFirm": "Ultra Seal Corporation",
"classification": "Class II",
"reasonForRecall": "cGMP deviations",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet packets, Mfg. for: Advanced First Aid, Baltimore MD 21237, American Safety & First Aid, Osceola, IN 46561, NDC 67060-210-68",
"distributionPattern": "Nationwide within the United States",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-24"
},
{
"city": "New Paltz",
"state": "NY",
"status": "Terminated",
"country": "United States",
"reportDate": "2022-02-09",
"productType": "Drugs",
"recallNumber": "D-0477-2022",
"recallingFirm": "Ultra Seal Corporation",
"classification": "Class II",
"reasonForRecall": "cGMP deviations",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Cetafen Non-aspirin pain reliever (acetaminophen 325mg) tablets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124",
"distributionPattern": "Nationwide within the United States",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-24"
},
{
"city": "New Paltz",
"state": "NY",
"status": "Terminated",
"country": "United States",
"reportDate": "2022-02-09",
"productType": "Drugs",
"recallNumber": "D-0488-2022",
"recallingFirm": "Ultra Seal Corporation",
"classification": "Class II",
"reasonForRecall": "cGMP deviations",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "PAIN TERMINATOR extra strength pain relief (aspirin 162 mg, acetaminophen 110 mg, Caffeine 32.4mg, Salicylamide 152 mg) 2 tablet packets, Manufactured for: Tellus Medical Products, Palm Desert, CA 92211, NDC 69103-2507",
"distributionPattern": "Nationwide within the United States",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-24"
},
{
"city": "New Paltz",
"state": "NY",
"status": "Terminated",
"country": "United States",
"reportDate": "2022-02-09",
"productType": "Drugs",
"recallNumber": "D-0485-2022",
"recallingFirm": "Ultra Seal Corporation",
"classification": "Class II",
"reasonForRecall": "cGMP deviations",
"voluntaryMandated": "Voluntary: Firm initiated",
"productDescription": "Pain Away Pain Reliever/Fever Reducer (NSAID) (acetaminophen 110 mg, aspirin 162 mg, salicylamide 152mg, caffeine 32.4 mg), 2 tablets per packet, Mfg, for Respond Industries and American First Aid, Mason, OH 45040",
"distributionPattern": "Nationwide within the United States",
"initialNotification": "Letter",
"recallInitiationDate": "2022-01-24"
}
],
"total": 59,
"source": {
"url": "https://open.fda.gov/apis/drug/enforcement/",
"license": "Public domain (US government records)",
"provider": "OpenFDA — Drug Recall Enforcement Reports"
}
},
"meta": {
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"tier": 0
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"caller": "x402",
"version": null,
"endpoint": "gov.fda-recalls",
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