{
  "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": "62511",
      "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": "Telephone",
      "distribution_pattern": "Distribution was nationwide, including Puerto Rico.  There was no foreign, military, or government distribution.",
      "recall_number": "D-083-2013",
      "product_description": "Levothroid (levothyroxine sodium tablets, USP), 137 mcg., 100-count bottles, Rx only, NDC 0456-1331-01,   Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.",
      "product_quantity": "36,978/100-tablet bottles",
      "reason_for_recall": "cGMP Deviations; does not meet in process specification requirements",
      "recall_initiation_date": "20120709",
      "center_classification_date": "20121203",
      "termination_date": "20131114",
      "report_date": "20121212",
      "code_info": "Lot #1095212 exp. 4/30/2013; and #1088877, exp. 11/30/2012"
    }
  ]
}