{
  "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": "Shenandoah",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62664",
      "recalling_firm": "Lloyd Inc. of Iowa",
      "address_1": "604 W Thomas Ave",
      "address_2": "N/A",
      "postal_code": "51601-1744",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution was nationwide and to Puerto Rico.  There was no foreign, military, or government distribution.",
      "recall_number": "D-103-2013",
      "product_description": "Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01,   Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.",
      "product_quantity": "16,548/100-tablet bottles",
      "reason_for_recall": "Subpotent; 9-month stability interval",
      "recall_initiation_date": "20120725",
      "center_classification_date": "20121221",
      "termination_date": "20131114",
      "report_date": "20130102",
      "code_info": "Lot 1094098, exp. date 9/2012"
    }
  ]
}