{
  "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-102-2013",
      "product_description": "Thyro-Tab 0.075 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA",
      "product_quantity": "1,924,133/75-mcg. tablets",
      "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 HF23111"
    }
  ]
}