{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gardena",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67265",
      "recalling_firm": "HUMAN SCIENCE FOUNDATION",
      "address_1": "13722 Harvard Pl",
      "address_2": "N/A",
      "postal_code": "90249-2527",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1327-2014",
      "product_description": "PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA",
      "product_quantity": "24,268 bottles",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin",
      "recall_initiation_date": "20140113",
      "center_classification_date": "20140519",
      "termination_date": "20140918",
      "report_date": "20140528",
      "code_info": "Lot# 220113; Exp. 01/16   Lot# 800213; Exp. 03/16  Lot# U133000; Exp. 04/16  Lot# U143200; Exp. 08/16  Lot# YJK015311; Exp. 10/16"
    }
  ]
}