{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Shenandoah",
      "address_1": "604 W Thomas Ave",
      "reason_for_recall": "Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.",
      "address_2": "",
      "product_quantity": "19,039 bottles",
      "code_info": "LOT NO.1092045",
      "center_classification_date": "20120622",
      "distribution_pattern": "Nationwide",
      "state": "IA",
      "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, Iowa 51601",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Lloyd Inc",
      "recall_number": "D-1394-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "61252",
      "termination_date": "20130730",
      "more_code_info": "",
      "recall_initiation_date": "20120224",
      "postal_code": "51601-1744",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}