{
  "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,
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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 9-month test interval.",
      "address_2": "Po Box 130",
      "product_quantity": "19,166 bottles",
      "code_info": "Lot 1087589",
      "center_classification_date": "20120622",
      "distribution_pattern": "Nationwide and PR.",
      "state": "IA",
      "product_description": "Levothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1321-01.  Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Lloyd Inc",
      "recall_number": "D-1393-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "61094",
      "termination_date": "20130730",
      "more_code_info": "",
      "recall_initiation_date": "20120203",
      "postal_code": "51601-1744",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}