{
  "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-076-2013",
      "product_description": "Thyro-Tab 0.088 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.",
      "product_quantity": "3,826,269 tablets",
      "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 #HA31411 and #HE17811"
    }
  ]
}